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nsv6652650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:123

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 215 SVs from 27 studies. See in: genome view    
    Submitted genomic6,174,797-6,174,919Question Mark
    Overlapping variant regions from other studies: 215 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):6,234,857-6,234,979Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6652650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr16,174,7976,174,919
    nsv6652650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr16,234,8576,234,979

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18630453duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18630453Submitted genomicNC_000001.11:g.617
    4797_6174919dup
    GRCh38 (hg38)NC_000001.11Chr16,174,7976,174,919
    nssv18630453RemappedPerfectNC_000001.10:g.623
    4857_6234979dup
    GRCh37.p13First PassNC_000001.10Chr16,234,8576,234,979

    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)
    nssv18630453<0.001152214892
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