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nsv5845149

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,200

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 26 studies. See in: genome view    
Submitted genomic3,365,122-3,366,321Question Mark
Overlapping variant regions from other studies: 172 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):3,365,356-3,366,555Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5845149Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr63,365,1223,366,321
nsv5845149RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr63,365,3563,366,555

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17505306copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17505306Submitted genomicGRCh38 (hg38)NC_000006.12Chr63,365,1223,366,321
nssv17505306RemappedPerfectGRCh37.p13First PassNC_000006.11Chr63,365,3563,366,555

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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