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nsv6394508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:636

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 26 studies. See in: genome view    
    Submitted genomic129,741,610-129,742,245Question Mark
    Overlapping variant regions from other studies: 122 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):130,662,765-130,663,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6394508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4129,741,610129,742,245
    nsv6394508RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4130,662,765130,663,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18111196deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18111196Submitted genomicNC_000004.12:g.129
    741610_129742245de
    l
    GRCh38 (hg38)NC_000004.12Chr4129,741,610129,742,245
    nssv18111196RemappedPerfectNC_000004.11:g.130
    662765_130663400de
    l
    GRCh37.p13First PassNC_000004.11Chr4130,662,765130,663,400

    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)
    nssv18111196<0.001437958
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