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nsv6953179

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:346,927

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 857 SVs from 74 studies. See in: genome view    
    Submitted genomic54,229,437-54,576,363Question Mark
    Overlapping variant regions from other studies: 857 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):54,696,155-55,043,081Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6953179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1454,229,43754,576,363
    nsv6953179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1454,696,15555,043,081

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616304duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616304Submitted genomicNC_000014.9:g.5422
    9437_54576363dup
    GRCh38 (hg38)NC_000014.9Chr1454,229,43754,576,363
    nssv18616304RemappedPerfectNC_000014.8:g.5469
    6155_55043081dup
    GRCh37.p13First PassNC_000014.8Chr1454,696,15555,043,081

    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)
    nssv186163044e-061273700
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