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nsv6748564

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 27 studies. See in: genome view    
    Submitted genomic141,685,068-141,685,179Question Mark
    Overlapping variant regions from other studies: 130 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):142,606,221-142,606,332Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6748564Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,685,068141,685,179
    nsv6748564RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,606,221142,606,332

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685223duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685223Submitted genomicNC_000004.12:g.141
    685068_141685179du
    p
    GRCh38 (hg38)NC_000004.12Chr4141,685,068141,685,179
    nssv18685223RemappedPerfectNC_000004.11:g.142
    606221_142606332du
    p
    GRCh37.p13First PassNC_000004.11Chr4142,606,221142,606,332

    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)
    nssv186852234e-061226176
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