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nsv5530601

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,012

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 276 SVs from 51 studies. See in: genome view    
Submitted genomic85,732,492-85,758,503Question Mark
Overlapping variant regions from other studies: 276 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):85,766,098-85,792,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530601Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1685,732,49285,758,503
nsv5530601RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1685,766,09885,792,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17708351deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17708351Submitted genomicNC_000016.10:g.857
32492_85758503del
GRCh38 (hg38)NC_000016.10Chr1685,732,49285,758,503
nssv17708351RemappedPerfectNC_000016.9:g.8576
6098_85792109del
GRCh37.p13First PassNC_000016.9Chr1685,766,09885,792,109

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)
nssv17708351<0.00116404
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