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nsv6723082

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:199,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1038 SVs from 70 studies. See in: genome view    
    Submitted genomic56,763,701-56,963,400Question Mark
    Overlapping variant regions from other studies: 1038 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):57,629,867-57,829,566Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6723082Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr456,763,70156,963,400
    nsv6723082RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr457,629,86757,829,566

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692902duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692902Submitted genomicNC_000004.12:g.567
    63701_56963400dup
    GRCh38 (hg38)NC_000004.12Chr456,763,70156,963,400
    nssv18692902RemappedPerfectNC_000004.11:g.576
    29867_57829566dup
    GRCh37.p13First PassNC_000004.11Chr457,629,86757,829,566

    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)
    nssv186929029.5e-0526267846
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