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nsv6390834

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 30 studies. See in: genome view    
    Submitted genomic133,183,901-133,190,000Question Mark
    Overlapping variant regions from other studies: 148 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):134,105,056-134,111,155Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6390834Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4133,183,901133,190,000
    nsv6390834RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4134,105,056134,111,155

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211049duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211049Submitted genomicNC_000004.12:g.133
    183901_133190000du
    p
    GRCh38 (hg38)NC_000004.12Chr4133,183,901133,190,000
    nssv18211049RemappedPerfectNC_000004.11:g.134
    105056_134111155du
    p
    GRCh37.p13First PassNC_000004.11Chr4134,105,056134,111,155

    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)
    nssv18211049<0.001138124
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