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nsv5528779

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:330

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view    
Submitted genomic58,140,525-58,140,854Question Mark
Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):58,651,892-58,652,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528779Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,140,52558,140,854
nsv5528779RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,651,89258,652,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724422duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724422Submitted genomicNC_000019.10:g.581
40525_58140854dup
GRCh38 (hg38)NC_000019.10Chr1958,140,52558,140,854
nssv17724422RemappedPerfectNC_000019.9:g.5865
1892_58652221dup
GRCh37.p13First PassNC_000019.9Chr1958,651,89258,652,221

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17724422<0.00116404
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