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nsv5524479

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,641

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
Submitted genomic37,140,825-37,144,465Question Mark
Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):35,769,228-35,772,868Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524479Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2037,140,82537,144,465
nsv5524479RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,769,22835,772,868

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732251deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732251Submitted genomicNC_000020.11:g.371
40825_37144465del
GRCh38 (hg38)NC_000020.11Chr2037,140,82537,144,465
nssv17732251RemappedPerfectNC_000020.10:g.357
69228_35772868del
GRCh37.p13First PassNC_000020.10Chr2035,769,22835,772,868

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)
nssv17732251<0.00116404
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