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nsv6917968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,052

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
    Submitted genomic66,648,756-66,650,807Question Mark
    Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):66,416,227-66,418,278Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6917968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,648,75666,650,807
    nsv6917968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,416,22766,418,278

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352116deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352116Submitted genomicNC_000011.10:g.666
    48756_66650807del
    GRCh38 (hg38)NC_000011.10Chr1166,648,75666,650,807
    nssv18352116RemappedPerfectNC_000011.9:g.6641
    6227_66418278del
    GRCh37.p13First PassNC_000011.9Chr1166,416,22766,418,278

    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)
    nssv183521167e-062275382
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