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nsv6990287

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:803,289

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2659 SVs from 87 studies. See in: genome view    
    Submitted genomic77,157,811-77,961,099Question Mark
    Overlapping variant regions from other studies: 2659 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):75,153,893-75,957,181Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990287Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,157,81177,961,099
    nsv6990287RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,153,89375,957,181

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631659duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631659Submitted genomicNC_000017.11:g.771
    57811_77961099dup
    GRCh38 (hg38)NC_000017.11Chr1777,157,81177,961,099
    nssv18631659RemappedPerfectNC_000017.10:g.751
    53893_75957181dup
    GRCh37.p13First PassNC_000017.10Chr1775,153,89375,957,181

    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)
    nssv186316594e-061275414
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