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nsv6972185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:178,745

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 426 SVs from 45 studies. See in: genome view    
    Submitted genomic71,361,263-71,540,007Question Mark
    Overlapping variant regions from other studies: 426 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):71,827,980-72,006,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1471,361,26371,540,007
    nsv6972185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,827,98072,006,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18389485deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18389485Submitted genomicNC_000014.9:g.7136
    1263_71540007del
    GRCh38 (hg38)NC_000014.9Chr1471,361,26371,540,007
    nssv18389485RemappedPerfectNC_000014.8:g.7182
    7980_72006724del
    GRCh37.p13First PassNC_000014.8Chr1471,827,98072,006,724

    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)
    nssv183894854e-061276244
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