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nsv6881604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,091

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 38 studies. See in: genome view    
    Submitted genomic49,357,491-49,381,581Question Mark
    Overlapping variant regions from other studies: 198 SVs from 39 studies. See in: genome view    
    Remapped(Score: Good):50,565,536-50,589,627Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6881604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1049,357,49149,381,581
    nsv6881604RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1050,565,53650,589,627

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18579420duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18579420Submitted genomicNC_000010.11:g.493
    57491_49381581dup
    GRCh38 (hg38)NC_000010.11Chr1049,357,49149,381,581
    nssv18579420RemappedGoodNC_000010.10:g.505
    65536_50589627dup
    GRCh37.p13First PassNC_000010.10Chr1050,565,53650,589,627

    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)
    nssv185794204e-061275922
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