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nsv6756574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,164

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 37 studies. See in: genome view    
    Submitted genomic142,409,264-142,417,427Question Mark
    Overlapping variant regions from other studies: 144 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):143,330,417-143,338,580Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6756574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4142,409,264142,417,427
    nsv6756574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4143,330,417143,338,580

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685270duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685270Submitted genomicNC_000004.12:g.142
    409264_142417427du
    p
    GRCh38 (hg38)NC_000004.12Chr4142,409,264142,417,427
    nssv18685270RemappedPerfectNC_000004.11:g.143
    330417_143338580du
    p
    GRCh37.p13First PassNC_000004.11Chr4143,330,417143,338,580

    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)
    nssv186852704e-061275492
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