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nsv6910720

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,397

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 24 studies. See in: genome view    
    Submitted genomic67,133,598-67,137,994Question Mark
    Overlapping variant regions from other studies: 85 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):66,901,069-66,905,465Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910720Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,133,59867,137,994
    nsv6910720RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,901,06966,905,465

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353086deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353086Submitted genomicNC_000011.10:g.671
    33598_67137994del
    GRCh38 (hg38)NC_000011.10Chr1167,133,59867,137,994
    nssv18353086RemappedPerfectNC_000011.9:g.6690
    1069_66905465del
    GRCh37.p13First PassNC_000011.9Chr1166,901,06966,905,465

    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)
    nssv183530862.5e-057275910
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