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nsv6640309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286,784

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1059 SVs from 69 studies. See in: genome view    
    Submitted genomic112,599,500-112,886,283Question Mark
    Overlapping variant regions from other studies: 1060 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):113,142,122-113,428,905Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,599,500112,886,283
    nsv6640309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,142,122113,428,905

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582251duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582251Submitted genomicNC_000001.11:g.112
    599500_112886283du
    p
    GRCh38 (hg38)NC_000001.11Chr1112,599,500112,886,283
    nssv18582251RemappedPerfectNC_000001.10:g.113
    142122_113428905du
    p
    GRCh37.p13First PassNC_000001.10Chr1113,142,122113,428,905

    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)
    nssv185822514e-061256234
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