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nsv6944378

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,808

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
    Submitted genomic61,070,605-61,077,412Question Mark
    Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):61,537,323-61,544,130Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6944378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1461,070,60561,077,412
    nsv6944378RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1461,537,32361,544,130

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617176duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617176Submitted genomicNC_000014.9:g.6107
    0605_61077412dup
    GRCh38 (hg38)NC_000014.9Chr1461,070,60561,077,412
    nssv18617176RemappedPerfectNC_000014.8:g.6153
    7323_61544130dup
    GRCh37.p13First PassNC_000014.8Chr1461,537,32361,544,130

    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)
    nssv186171761.1e-053275076
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