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nsv6743165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:328,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1212 SVs from 67 studies. See in: genome view    
    Submitted genomic86,842,201-87,170,600Question Mark
    Overlapping variant regions from other studies: 1212 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):87,763,354-88,091,752Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6743165Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr486,842,20187,170,600
    nsv6743165RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr487,763,35488,091,752

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691466duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691466Submitted genomicNC_000004.12:g.868
    42201_87170600dup
    GRCh38 (hg38)NC_000004.12Chr486,842,20187,170,600
    nssv18691466RemappedPerfectNC_000004.11:g.877
    63354_88091752dup
    GRCh37.p13First PassNC_000004.11Chr487,763,35488,091,752

    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)
    nssv186914664e-061275506
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