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nsv6665182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:172,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 585 SVs from 66 studies. See in: genome view    
    Submitted genomic43,630,394-43,803,065Question Mark
    Overlapping variant regions from other studies: 585 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):43,857,533-44,030,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6665182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr243,630,39443,803,065
    nsv6665182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr243,857,53344,030,204

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664621duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664621Submitted genomicNC_000002.12:g.436
    30394_43803065dup
    GRCh38 (hg38)NC_000002.12Chr243,630,39443,803,065
    nssv18664621RemappedPerfectNC_000002.11:g.438
    57533_44030204dup
    GRCh37.p13First PassNC_000002.11Chr243,857,53344,030,204

    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)
    nssv186646214e-061274700
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