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nsv6970618

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 408 SVs from 40 studies. See in: genome view    
    Submitted genomic1,072,013-1,072,043Question Mark
    Overlapping variant regions from other studies: 408 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):1,122,013-1,122,043Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970618Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,072,0131,072,043
    nsv6970618RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,122,0131,122,043

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400096deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400096Submitted genomicNC_000016.10:g.107
    2013_1072043del
    GRCh38 (hg38)NC_000016.10Chr161,072,0131,072,043
    nssv18400096RemappedPerfectNC_000016.9:g.1122
    013_1122043del
    GRCh37.p13First PassNC_000016.9Chr161,122,0131,122,043

    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)
    nssv184000960.30468006223498
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