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nsv6810871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:661,079

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2047 SVs from 95 studies. See in: genome view    
    Submitted genomic16,504,503-17,165,581Question Mark
    Overlapping variant regions from other studies: 2047 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):16,544,128-17,205,205Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6810871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,504,50317,165,581
    nsv6810871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,544,12817,205,205

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723502duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723502Submitted genomicNC_000007.14:g.165
    04503_17165581dup
    GRCh38 (hg38)NC_000007.14Chr716,504,50317,165,581
    nssv18723502RemappedPerfectNC_000007.13:g.165
    44128_17205205dup
    GRCh37.p13First PassNC_000007.13Chr716,544,12817,205,205

    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)
    nssv187235027e-062275264
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