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nsv6836712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,701

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Submitted genomic80,892,976-80,894,676Question Mark
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):80,522,292-80,523,992Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6836712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr780,892,97680,894,676
    nsv6836712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr780,522,29280,523,992

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18728898duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18728898Submitted genomicNC_000007.14:g.808
    92976_80894676dup
    GRCh38 (hg38)NC_000007.14Chr780,892,97680,894,676
    nssv18728898RemappedPerfectNC_000007.13:g.805
    22292_80523992dup
    GRCh37.p13First PassNC_000007.13Chr780,522,29280,523,992

    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)
    nssv187288984e-061270328
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