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nsv6387755

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,049

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 39 studies. See in: genome view    
    Submitted genomic163,092,479-163,107,527Question Mark
    Overlapping variant regions from other studies: 182 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):164,013,631-164,028,679Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6387755Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4163,092,479163,107,527
    nsv6387755RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4164,013,631164,028,679

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18113755deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18113755Submitted genomicNC_000004.12:g.163
    092479_163107527de
    l
    GRCh38 (hg38)NC_000004.12Chr4163,092,479163,107,527
    nssv18113755RemappedPerfectNC_000004.11:g.164
    013631_164028679de
    l
    GRCh37.p13First PassNC_000004.11Chr4164,013,631164,028,679

    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)
    nssv18113755<0.001239256
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