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nsv6650776

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Submitted genomic46,875,901-46,882,000Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):47,341,573-47,347,672Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650776Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,875,90146,882,000
    nsv6650776RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr147,341,57347,347,672

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18390980deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18390980Submitted genomicNC_000001.11:g.468
    75901_46882000del
    GRCh38 (hg38)NC_000001.11Chr146,875,90146,882,000
    nssv18390980RemappedPerfectNC_000001.10:g.473
    41573_47347672del
    GRCh37.p13First PassNC_000001.10Chr147,341,57347,347,672

    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)
    nssv183909805e-0513253006
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