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nsv6912914

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:279,915

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 994 SVs from 91 studies. See in: genome view    
    Submitted genomic67,707,301-67,987,215Question Mark
    Overlapping variant regions from other studies: 992 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):67,474,772-67,754,686Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912914Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,707,30167,987,215
    nsv6912914RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,474,77267,754,686

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353132deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353132Submitted genomicNC_000011.10:g.677
    07301_67987215del
    GRCh38 (hg38)NC_000011.10Chr1167,707,30167,987,215
    nssv18353132RemappedPerfectNC_000011.9:g.6747
    4772_67754686del
    GRCh37.p13First PassNC_000011.9Chr1167,474,77267,754,686

    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)
    nssv183531320.002516253950
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