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nsv6386644

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:609

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 22 studies. See in: genome view    
    Submitted genomic129,749,246-129,749,854Question Mark
    Overlapping variant regions from other studies: 120 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):130,670,401-130,671,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6386644Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4129,749,246129,749,854
    nsv6386644RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4130,670,401130,671,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18111197deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18111197Submitted genomicNC_000004.12:g.129
    749246_129749854de
    l
    GRCh38 (hg38)NC_000004.12Chr4129,749,246129,749,854
    nssv18111197RemappedPerfectNC_000004.11:g.130
    670401_130671009de
    l
    GRCh37.p13First PassNC_000004.11Chr4130,670,401130,671,009

    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)
    nssv18111197<0.001737908
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