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nsv7031337

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
    Submitted genomic61,716,401-61,716,700Question Mark
    Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):60,291,457-60,291,756Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7031337Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2061,716,40161,716,700
    nsv7031337RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2060,291,45760,291,756

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645300duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645300Submitted genomicNC_000020.11:g.617
    16401_61716700dup
    GRCh38 (hg38)NC_000020.11Chr2061,716,40161,716,700
    nssv18645300RemappedPerfectNC_000020.10:g.602
    91457_60291756dup
    GRCh37.p13First PassNC_000020.10Chr2060,291,45760,291,756

    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)
    nssv186453004e-061232888
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