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nsv6389066

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:162

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Submitted genomic145,101,579-145,101,740Question Mark
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):146,022,731-146,022,892Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6389066Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4145,101,579145,101,740
    nsv6389066RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4146,022,731146,022,892

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18108857deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18108857Submitted genomicNC_000004.12:g.145
    101579_145101740de
    l
    GRCh38 (hg38)NC_000004.12Chr4145,101,579145,101,740
    nssv18108857RemappedPerfectNC_000004.11:g.146
    022731_146022892de
    l
    GRCh37.p13First PassNC_000004.11Chr4146,022,731146,022,892

    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)
    nssv181088570.0015537354
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