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nsv6975719

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,175

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 281 SVs from 43 studies. See in: genome view    
    Submitted genomic59,681,182-59,727,356Question Mark
    Overlapping variant regions from other studies: 281 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):59,973,381-60,019,555Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975719Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,681,18259,727,356
    nsv6975719RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,973,38160,019,555

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620295duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620295Submitted genomicNC_000015.10:g.596
    81182_59727356dup
    GRCh38 (hg38)NC_000015.10Chr1559,681,18259,727,356
    nssv18620295RemappedPerfectNC_000015.9:g.5997
    3381_60019555dup
    GRCh37.p13First PassNC_000015.9Chr1559,973,38160,019,555

    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)
    nssv186202951.1e-053276008
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