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nsv7000686

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,122

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 204 SVs from 43 studies. See in: genome view    
    Submitted genomic36,094,511-36,127,632Question Mark
    Overlapping variant regions from other studies: 204 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):36,585,413-36,618,534Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000686Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,094,51136,127,632
    nsv7000686RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,585,41336,618,534

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637840duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637840Submitted genomicNC_000019.10:g.360
    94511_36127632dup
    GRCh38 (hg38)NC_000019.10Chr1936,094,51136,127,632
    nssv18637840RemappedPerfectNC_000019.9:g.3658
    5413_36618534dup
    GRCh37.p13First PassNC_000019.9Chr1936,585,41336,618,534

    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)
    nssv186378407e-062275942
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