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nsv6639992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 31 studies. See in: genome view    
    Submitted genomic112,676,901-112,681,900Question Mark
    Overlapping variant regions from other studies: 156 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):113,219,523-113,224,522Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6639992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,676,901112,681,900
    nsv6639992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,219,523113,224,522

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18346925deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18346925Submitted genomicNC_000001.11:g.112
    676901_112681900de
    l
    GRCh38 (hg38)NC_000001.11Chr1112,676,901112,681,900
    nssv18346925RemappedPerfectNC_000001.10:g.113
    219523_113224522de
    l
    GRCh37.p13First PassNC_000001.10Chr1113,219,523113,224,522

    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)
    nssv183469250.004891253132
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