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nsv6966456

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,859

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 223 SVs from 50 studies. See in: genome view    
    Submitted genomic43,352,096-43,393,954Question Mark
    Overlapping variant regions from other studies: 223 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):43,644,294-43,686,152Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966456Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,352,09643,393,954
    nsv6966456RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,644,29443,686,152

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619470duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619470Submitted genomicNC_000015.10:g.433
    52096_43393954dup
    GRCh38 (hg38)NC_000015.10Chr1543,352,09643,393,954
    nssv18619470RemappedPerfectNC_000015.9:g.4364
    4294_43686152dup
    GRCh37.p13First PassNC_000015.9Chr1543,644,29443,686,152

    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)
    nssv186194701.4e-054274974
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