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nsv6538774

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:327,591

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1058 SVs from 76 studies. See in: genome view    
    Submitted genomic29,445,909-29,773,499Question Mark
    Overlapping variant regions from other studies: 1058 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):29,841,898-30,169,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6538774Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2229,445,90929,773,499
    nsv6538774RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2229,841,89830,169,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18204975duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18204975Submitted genomicNC_000022.11:g.294
    45909_29773499dup
    GRCh38 (hg38)NC_000022.11Chr2229,445,90929,773,499
    nssv18204975RemappedPerfectNC_000022.10:g.298
    41898_30169488dup
    GRCh37.p13First PassNC_000022.10Chr2229,841,89830,169,488

    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)
    nssv18204975<0.001139290
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