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nsv6992677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:275,979

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 797 SVs from 73 studies. See in: genome view    
    Submitted genomic30,859,398-31,135,376Question Mark
    Overlapping variant regions from other studies: 797 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):30,870,719-31,146,697Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1630,859,39831,135,376
    nsv6992677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1630,870,71931,146,697

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18399023deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18399023Submitted genomicNC_000016.10:g.308
    59398_31135376del
    GRCh38 (hg38)NC_000016.10Chr1630,859,39831,135,376
    nssv18399023RemappedPerfectNC_000016.9:g.3087
    0719_31146697del
    GRCh37.p13First PassNC_000016.9Chr1630,870,71931,146,697

    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)
    nssv183990234e-061276150
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