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nsv6484639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 20 studies. See in: genome view    
    Submitted genomic38,254,501-38,256,500Question Mark
    Overlapping variant regions from other studies: 89 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):38,723,706-38,725,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6484639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1438,254,50138,256,500
    nsv6484639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1438,723,70638,725,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18196854duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18196854Submitted genomicNC_000014.9:g.3825
    4501_38256500dup
    GRCh38 (hg38)NC_000014.9Chr1438,254,50138,256,500
    nssv18196854RemappedPerfectNC_000014.8:g.3872
    3706_38725705dup
    GRCh37.p13First PassNC_000014.8Chr1438,723,70638,725,705

    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)
    nssv18196854<0.001238878
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