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nsv5517938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,020

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 322 SVs from 49 studies. See in: genome view    
Submitted genomic82,149,966-82,195,985Question Mark
Overlapping variant regions from other studies: 322 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):82,183,571-82,229,590Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1682,149,96682,195,985
nsv5517938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1682,183,57182,229,590

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709576deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709576Submitted genomicNC_000016.10:g.821
49966_82195985del
GRCh38 (hg38)NC_000016.10Chr1682,149,96682,195,985
nssv17709576RemappedPerfectNC_000016.9:g.8218
3571_82229590del
GRCh37.p13First PassNC_000016.9Chr1682,183,57182,229,590

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)
nssv17709576<0.00126404
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