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nsv6382691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 38 studies. See in: genome view    
    Submitted genomic128,283,501-128,291,600Question Mark
    Overlapping variant regions from other studies: 153 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):129,204,656-129,212,755Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6382691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4128,283,501128,291,600
    nsv6382691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4129,204,656129,212,755

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18210301duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18210301Submitted genomicNC_000004.12:g.128
    283501_128291600du
    p
    GRCh38 (hg38)NC_000004.12Chr4128,283,501128,291,600
    nssv18210301RemappedPerfectNC_000004.11:g.129
    204656_129212755du
    p
    GRCh37.p13First PassNC_000004.11Chr4129,204,656129,212,755

    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)
    nssv18210301<0.001139242
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