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nsv6962425

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:759,167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11426 SVs from 115 studies. See in: genome view    
    Submitted genomic105,863,194-106,622,360Question Mark
    Overlapping variant regions from other studies: 6475 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):526,361-1,285,527Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962425Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14105,863,194106,622,360
    nsv6962425RemappedPerfectGRCh37.p13PATCHESSecond PassNW_004166863.1Chr14|NW_0
    04166863.1
    526,3611,285,527

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18384720deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18384720Submitted genomicNC_000014.9:g.1058
    63194_106622360del
    GRCh38 (hg38)NC_000014.9Chr14105,863,194106,622,360
    nssv18384720RemappedPerfectNW_004166863.1:g.5
    26361_1285527del
    GRCh37.p13Second PassNW_004166863.1Chr14|NW_0
    04166863.1
    526,3611,285,527

    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)
    nssv18384720<0.00163200346
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