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nsv6456183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,908

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 328 SVs from 55 studies. See in: genome view    
    Submitted genomic9,964,309-10,014,216Question Mark
    Overlapping variant regions from other studies: 329 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):10,116,908-10,166,815Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6456183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,964,30910,014,216
    nsv6456183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,116,90810,166,815

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188528duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188528Submitted genomicNC_000012.12:g.996
    4309_10014216dup
    GRCh38 (hg38)NC_000012.12Chr129,964,30910,014,216
    nssv18188528RemappedPerfectNC_000012.11:g.101
    16908_10166815dup
    GRCh37.p13First PassNC_000012.11Chr1210,116,90810,166,815

    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)
    nssv18188528<0.001139288
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