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nsv6670871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,624

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 207 SVs from 42 studies. See in: genome view    
    Submitted genomic64,891,390-64,922,013Question Mark
    Overlapping variant regions from other studies: 207 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):65,118,524-65,149,147Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6670871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr264,891,39064,922,013
    nsv6670871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr265,118,52465,149,147

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666566duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666566Submitted genomicNC_000002.12:g.648
    91390_64922013dup
    GRCh38 (hg38)NC_000002.12Chr264,891,39064,922,013
    nssv18666566RemappedPerfectNC_000002.11:g.651
    18524_65149147dup
    GRCh37.p13First PassNC_000002.11Chr265,118,52465,149,147

    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)
    nssv186665664e-061275456
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