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nsv6958407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62,219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 256 SVs from 50 studies. See in: genome view    
    Submitted genomic82,255,211-82,317,429Question Mark
    Overlapping variant regions from other studies: 260 SVs from 51 studies. See in: genome view    
    Remapped(Score: Good):82,547,552-82,609,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6958407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1582,255,21182,317,429
    nsv6958407RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1582,547,55282,609,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620610duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620610Submitted genomicNC_000015.10:g.822
    55211_82317429dup
    GRCh38 (hg38)NC_000015.10Chr1582,255,21182,317,429
    nssv18620610RemappedGoodNC_000015.9:g.8254
    7552_82609765dup
    GRCh37.p13First PassNC_000015.9Chr1582,547,55282,609,765

    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)
    nssv186206104e-061273080
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