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nsv6959604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:277,984

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 772 SVs from 63 studies. See in: genome view    
    Submitted genomic88,482,877-88,760,860Question Mark
    Overlapping variant regions from other studies: 772 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):88,949,221-89,227,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6959604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1488,482,87788,760,860
    nsv6959604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1488,949,22189,227,204

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615212duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615212Submitted genomicNC_000014.9:g.8848
    2877_88760860dup
    GRCh38 (hg38)NC_000014.9Chr1488,482,87788,760,860
    nssv18615212RemappedPerfectNC_000014.8:g.8894
    9221_89227204dup
    GRCh37.p13First PassNC_000014.8Chr1488,949,22189,227,204

    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)
    nssv186152124e-061274610
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