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nsv6898152

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 66 SVs from 12 studies. See in: genome view    
    Submitted genomic72,135,925-72,135,961Question Mark
    Overlapping variant regions from other studies: 66 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):71,846,971-71,847,007Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6898152Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1172,135,92572,135,961
    nsv6898152RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1171,846,97171,847,007

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352149deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352149Submitted genomicNC_000011.10:g.721
    35925_72135961del
    GRCh38 (hg38)NC_000011.10Chr1172,135,92572,135,961
    nssv18352149RemappedPerfectNC_000011.9:g.7184
    6971_71847007del
    GRCh37.p13First PassNC_000011.9Chr1171,846,97171,847,007

    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)
    nssv183521490.003775247120
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