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esv2759411

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:203,631

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 583 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):29,501,324-29,704,888Question Mark
Overlapping variant regions from other studies: 34 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):766,699-970,251Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):766,790-970,387Question Mark
Overlapping variant regions from other studies: 26 SVs from 4 studies. See in: genome view    
Remapped(Score: Good):810,335-1,013,923Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):766,449-970,001Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):766,847-970,432Question Mark
Overlapping variant regions from other studies: 33 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):987,776-1,191,406Question Mark
Overlapping variant regions from other studies: 23 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):766,985-964,446Question Mark
Overlapping variant regions from other studies: 583 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):29,469,101-29,672,665Question Mark
Overlapping variant regions from other studies: 33 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):987,882-1,191,512Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):772,432-976,017Question Mark
Overlapping variant regions from other studies: 34 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):772,284-975,836Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):772,386-975,983Question Mark
Overlapping variant regions from other studies: 26 SVs from 4 studies. See in: genome view    
Remapped(Score: Good):809,633-1,013,221Question Mark
Overlapping variant regions from other studies: 23 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):772,579-970,040Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Good):772,069-975,621Question Mark
Overlapping variant regions from other studies: 36 SVs from 6 studies. See in: genome view    
Submitted genomic29,577,080-29,780,644Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2759411RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr629,501,32429,704,888
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_5Second PassNT_167247.2Chr6|NT_16
7247.2		766,699970,251
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_6Second PassNT_167248.2Chr6|NT_16
7248.2		766,790970,387
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_7Second PassNT_167249.2Chr6|NT_16
7249.2		810,3351,013,923
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_4Second PassNT_167246.2Chr6|NT_16
7246.2		766,449970,001
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_3Second PassNT_167245.2Chr6|NT_16
7245.2		766,847970,432
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_2Second PassNT_113891.3Chr6|NT_11
3891.3		987,7761,191,406
esv2759411RemappedGoodGRCh38.p12ALT_REF_LOCI_1Second PassNT_167244.2Chr6|NT_16
7244.2		766,985964,446
esv2759411RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,469,10129,672,665
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_2Second PassNT_113891.2Chr6|NT_11
3891.2		987,8821,191,512
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_3Second PassNT_167245.1Chr6|NT_16
7245.1		772,432976,017
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_5Second PassNT_167247.1Chr6|NT_16
7247.1		772,284975,836
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_6Second PassNT_167248.1Chr6|NT_16
7248.1		772,386975,983
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_7Second PassNT_167249.1Chr6|NT_16
7249.1		809,6331,013,221
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_1Second PassNT_167244.1Chr6|NT_16
7244.1		772,579970,040
esv2759411RemappedGoodGRCh37.p13ALT_REF_LOCI_4Second PassNT_167246.1Chr6|NT_16
7246.1		772,069975,621
esv2759411Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000006.9Chr629,577,08029,780,644

Variant Call Information

Variant Call IDTypeMethod
esv2758039copy number variationMerged region

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrInner StartInner Stop
esv2758039RemappedGoodGRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2		766,449970,001
esv2758039RemappedGoodGRCh38.p12Second PassNT_167247.2Chr6|NT_16
7247.2		766,699970,251
esv2758039RemappedGoodGRCh38.p12Second PassNT_167248.2Chr6|NT_16
7248.2		766,790970,387
esv2758039RemappedGoodGRCh38.p12Second PassNT_167249.2Chr6|NT_16
7249.2		810,3351,013,923
esv2758039RemappedGoodGRCh38.p12Second PassNT_167245.2Chr6|NT_16
7245.2		766,847970,432
esv2758039RemappedGoodGRCh38.p12Second PassNT_167244.2Chr6|NT_16
7244.2		766,985964,446
esv2758039RemappedGoodGRCh38.p12Second PassNT_113891.3Chr6|NT_11
3891.3		987,7761,191,406
esv2758039RemappedPerfectGRCh38.p12First PassNC_000006.12Chr629,501,32429,704,888
esv2758039RemappedGoodGRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1		772,069975,621
esv2758039RemappedGoodGRCh37.p13Second PassNT_167247.1Chr6|NT_16
7247.1		772,284975,836
esv2758039RemappedGoodGRCh37.p13Second PassNT_167248.1Chr6|NT_16
7248.1		772,386975,983
esv2758039RemappedGoodGRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		772,432976,017
esv2758039RemappedGoodGRCh37.p13Second PassNT_167244.1Chr6|NT_16
7244.1		772,579970,040
esv2758039RemappedGoodGRCh37.p13Second PassNT_167249.1Chr6|NT_16
7249.1		809,6331,013,221
esv2758039RemappedGoodGRCh37.p13Second PassNT_113891.2Chr6|NT_11
3891.2		987,8821,191,512
esv2758039RemappedPerfectGRCh37.p13First PassNC_000006.11Chr629,469,10129,672,665
esv2758039Submitted genomicNCBI35 (hg17)NC_000006.9Chr629,577,08029,780,644

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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