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nsv6810011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:370,910

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1456 SVs from 92 studies. See in: genome view    
    Submitted genomic25,848,777-26,219,686Question Mark
    Overlapping variant regions from other studies: 1456 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):25,888,397-26,259,306Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6810011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr725,848,77726,219,686
    nsv6810011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr725,888,39726,259,306

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723332duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723332Submitted genomicNC_000007.14:g.258
    48777_26219686dup
    GRCh38 (hg38)NC_000007.14Chr725,848,77726,219,686
    nssv18723332RemappedPerfectNC_000007.13:g.258
    88397_26259306dup
    GRCh37.p13First PassNC_000007.13Chr725,888,39726,259,306

    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)
    nssv187233324e-061275756
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