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nsv6609908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,158

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
    Submitted genomic99,341,202-99,343,359Question Mark
    Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):98,938,825-98,940,982Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6609908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,341,20299,343,359
    nsv6609908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr798,938,82598,940,982

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18161335deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18161335Submitted genomicNC_000007.14:g.993
    41202_99343359del
    GRCh38 (hg38)NC_000007.14Chr799,341,20299,343,359
    nssv18161335RemappedPerfectNC_000007.13:g.989
    38825_98940982del
    GRCh37.p13First PassNC_000007.13Chr798,938,82598,940,982

    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)
    nssv18161335<0.001138622
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