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nsv6509140

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:239

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
    Submitted genomic16,157,692-16,157,930Question Mark
    Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):16,061,006-16,061,244Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6509140Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1716,157,69216,157,930
    nsv6509140RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1716,061,00616,061,244

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18034589deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18034589Submitted genomicNC_000017.11:g.161
    57692_16157930del
    GRCh38 (hg38)NC_000017.11Chr1716,157,69216,157,930
    nssv18034589RemappedPerfectNC_000017.10:g.160
    61006_16061244del
    GRCh37.p13First PassNC_000017.10Chr1716,061,00616,061,244

    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)
    nssv18034589<0.001733076
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