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nsv6827180

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:571,784

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1162 SVs from 81 studies. See in: genome view    
    Submitted genomic116,747,495-117,319,278Question Mark
    Overlapping variant regions from other studies: 1162 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):116,387,549-116,959,332Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6827180Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7116,747,495117,319,278
    nsv6827180RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7116,387,549116,959,332

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18721462duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18721462Submitted genomicNC_000007.14:g.116
    747495_117319278du
    p
    GRCh38 (hg38)NC_000007.14Chr7116,747,495117,319,278
    nssv18721462RemappedPerfectNC_000007.13:g.116
    387549_116959332du
    p
    GRCh37.p13First PassNC_000007.13Chr7116,387,549116,959,332

    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)
    nssv187214624e-061275788
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