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nsv6983060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 269 SVs from 34 studies. See in: genome view    
    Submitted genomic82,048,825-82,048,918Question Mark
    Overlapping variant regions from other studies: 269 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):80,006,701-80,006,794Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,048,82582,048,918
    nsv6983060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1780,006,70180,006,794

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631578duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631578Submitted genomicNC_000017.11:g.820
    48825_82048918dup
    GRCh38 (hg38)NC_000017.11Chr1782,048,82582,048,918
    nssv18631578RemappedPerfectNC_000017.10:g.800
    06701_80006794dup
    GRCh37.p13First PassNC_000017.10Chr1780,006,70180,006,794

    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)
    nssv18631578<0.00130225290
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