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nsv6807204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,355

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 530 SVs from 74 studies. See in: genome view    
    Submitted genomic16,822,353-16,907,707Question Mark
    Overlapping variant regions from other studies: 530 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):16,861,977-16,947,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6807204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,822,35316,907,707
    nsv6807204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,861,97716,947,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18538699deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18538699Submitted genomicNC_000007.14:g.168
    22353_16907707del
    GRCh38 (hg38)NC_000007.14Chr716,822,35316,907,707
    nssv18538699RemappedPerfectNC_000007.13:g.168
    61977_16947331del
    GRCh37.p13First PassNC_000007.13Chr716,861,97716,947,331

    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)
    nssv185386994e-061276216
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