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nsv6677370

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,519,056

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2957 SVs from 85 studies. See in: genome view    
    Submitted genomic20,792,052-22,311,107Question Mark
    Overlapping variant regions from other studies: 2961 SVs from 85 studies. See in: genome view    
    Remapped(Score: Good):20,991,812-22,533,979Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6677370Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr220,792,05222,311,107
    nsv6677370RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr220,991,81222,533,979

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18660900duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18660900Submitted genomicNC_000002.12:g.207
    92052_22311107dup
    GRCh38 (hg38)NC_000002.12Chr220,792,05222,311,107
    nssv18660900RemappedGoodNC_000002.11:g.209
    91812_22533979dup
    GRCh37.p13First PassNC_000002.11Chr220,991,81222,533,979

    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)
    nssv186609004e-061271620
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