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nsv6980162

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139,923

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 938 SVs from 74 studies. See in: genome view    
    Submitted genomic82,276,139-82,416,061Question Mark
    Overlapping variant regions from other studies: 938 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):80,234,015-80,373,937Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980162Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,276,13982,416,061
    nsv6980162RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1780,234,01580,373,937

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631600duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631600Submitted genomicNC_000017.11:g.822
    76139_82416061dup
    GRCh38 (hg38)NC_000017.11Chr1782,276,13982,416,061
    nssv18631600RemappedPerfectNC_000017.10:g.802
    34015_80373937dup
    GRCh37.p13First PassNC_000017.10Chr1780,234,01580,373,937

    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)
    nssv18631600<0.001126274426
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