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nsv6695687

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 14 studies. See in: genome view    
    Submitted genomic230,957,515-230,957,598Question Mark
    Overlapping variant regions from other studies: 78 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):231,822,230-231,822,313Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6695687Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2230,957,515230,957,598
    nsv6695687RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,822,230231,822,313

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664969duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664969Submitted genomicNC_000002.12:g.230
    957515_230957598du
    p
    GRCh38 (hg38)NC_000002.12Chr2230,957,515230,957,598
    nssv18664969RemappedPerfectNC_000002.11:g.231
    822230_231822313du
    p
    GRCh37.p13First PassNC_000002.11Chr2231,822,230231,822,313

    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)
    nssv18664969<0.001167214270
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