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nsv6960749

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,925

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Submitted genomic65,122,991-65,124,915Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):65,415,329-65,417,253Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,122,99165,124,915
    nsv6960749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,415,32965,417,253

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18618245duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18618245Submitted genomicNC_000015.10:g.651
    22991_65124915dup
    GRCh38 (hg38)NC_000015.10Chr1565,122,99165,124,915
    nssv18618245RemappedPerfectNC_000015.9:g.6541
    5329_65417253dup
    GRCh37.p13First PassNC_000015.9Chr1565,415,32965,417,253

    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)
    nssv186182451.8e-055270718
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