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nsv6677483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,575

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 229 SVs from 52 studies. See in: genome view    
    Submitted genomic3,654,730-3,676,304Question Mark
    Overlapping variant regions from other studies: 229 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):3,702,320-3,723,894Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6677483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr23,654,7303,676,304
    nsv6677483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr23,702,3203,723,894

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663304duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663304Submitted genomicNC_000002.12:g.365
    4730_3676304dup
    GRCh38 (hg38)NC_000002.12Chr23,654,7303,676,304
    nssv18663304RemappedPerfectNC_000002.11:g.370
    2320_3723894dup
    GRCh37.p13First PassNC_000002.11Chr23,702,3203,723,894

    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)
    nssv186633044e-061275518
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