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nsv7035258

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,291,797

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3274 SVs from 94 studies. See in: genome view    
    Submitted genomic24,250,776-25,542,572Question Mark
    Overlapping variant regions from other studies: 3274 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):24,231,412-25,523,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035258Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2024,250,77625,542,572
    nsv7035258RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2024,231,41225,523,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642709duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642709Submitted genomicNC_000020.11:g.242
    50776_25542572dup
    GRCh38 (hg38)NC_000020.11Chr2024,250,77625,542,572
    nssv18642709RemappedPerfectNC_000020.10:g.242
    31412_25523208dup
    GRCh37.p13First PassNC_000020.10Chr2024,231,41225,523,208

    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)
    nssv186427094e-061272930
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