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nsv5523328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 31 studies. See in: genome view    
Submitted genomic89,629,240-89,629,349Question Mark
Overlapping variant regions from other studies: 154 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):90,172,471-90,172,580Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1589,629,24089,629,349
nsv5523328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1590,172,47190,172,580

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704132deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704132Submitted genomicNC_000015.10:g.896
29240_89629349del
GRCh38 (hg38)NC_000015.10Chr1589,629,24089,629,349
nssv17704132RemappedPerfectNC_000015.9:g.9017
2471_90172580del
GRCh37.p13First PassNC_000015.9Chr1590,172,47190,172,580

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)
nssv177041320.003216390
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