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nsv6794764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112,006

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 925 SVs from 79 studies. See in: genome view    
    Submitted genomic181,111,369-181,223,374Question Mark
    Overlapping variant regions from other studies: 925 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):180,538,369-180,650,374Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6794764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,111,369181,223,374
    nsv6794764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,538,369180,650,374

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18702232duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18702232Submitted genomicNC_000005.10:g.181
    111369_181223374du
    p
    GRCh38 (hg38)NC_000005.10Chr5181,111,369181,223,374
    nssv18702232RemappedPerfectNC_000005.9:g.1805
    38369_180650374dup
    GRCh37.p13First PassNC_000005.9Chr5180,538,369180,650,374

    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)
    nssv187022324e-061275668
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