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nsv6904054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,131

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 478 SVs from 57 studies. See in: genome view    
    Submitted genomic67,060,113-67,166,243Question Mark
    Overlapping variant regions from other studies: 478 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):66,827,584-66,933,714Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6904054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,060,11367,166,243
    nsv6904054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,827,58466,933,714

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582218duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582218Submitted genomicNC_000011.10:g.670
    60113_67166243dup
    GRCh38 (hg38)NC_000011.10Chr1167,060,11367,166,243
    nssv18582218RemappedPerfectNC_000011.9:g.6682
    7584_66933714dup
    GRCh37.p13First PassNC_000011.9Chr1166,827,58466,933,714

    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)
    nssv185822184e-061275532
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