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nsv6794151

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Submitted genomic53,037,891-53,043,892Question Mark
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):52,902,689-52,908,690Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6794151Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr653,037,89153,043,892
    nsv6794151RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr652,902,68952,908,690

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18716759duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18716759Submitted genomicNC_000006.12:g.530
    37891_53043892dup
    GRCh38 (hg38)NC_000006.12Chr653,037,89153,043,892
    nssv18716759RemappedPerfectNC_000006.11:g.529
    02689_52908690dup
    GRCh37.p13First PassNC_000006.11Chr652,902,68952,908,690

    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)
    nssv187167591.1e-053275494
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