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nsv6972108

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
    Submitted genomic87,976,201-87,980,400Question Mark
    Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):88,442,545-88,446,744Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1487,976,20187,980,400
    nsv6972108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1488,442,54588,446,744

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615186duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615186Submitted genomicNC_000014.9:g.8797
    6201_87980400dup
    GRCh38 (hg38)NC_000014.9Chr1487,976,20187,980,400
    nssv18615186RemappedPerfectNC_000014.8:g.8844
    2545_88446744dup
    GRCh37.p13First PassNC_000014.8Chr1488,442,54588,446,744

    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)
    nssv186151864e-061273454
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