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nsv7005713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,263,097

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19984 SVs from 125 studies. See in: genome view    
    Submitted genomic33,458,650-39,721,746Question Mark
    Overlapping variant regions from other studies: 19980 SVs from 125 studies. See in: genome view    
    Remapped(Score: Good):33,949,556-40,212,386Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1933,458,65039,721,746
    nsv7005713RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1933,949,55640,212,386

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424802deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424802Submitted genomicNC_000019.10:g.334
    58650_39721746del
    GRCh38 (hg38)NC_000019.10Chr1933,458,65039,721,746
    nssv18424802RemappedGoodNC_000019.9:g.3394
    9556_40212386del
    GRCh37.p13First PassNC_000019.9Chr1933,949,55640,212,386

    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)
    nssv184248024e-061275594
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