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nsv6650228

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,839

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 418 SVs from 46 studies. See in: genome view    
    Submitted genomic43,699,713-43,809,551Question Mark
    Overlapping variant regions from other studies: 418 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):44,165,384-44,275,222Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650228Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr143,699,71343,809,551
    nsv6650228RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,165,38444,275,222

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18629181duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18629181Submitted genomicNC_000001.11:g.436
    99713_43809551dup
    GRCh38 (hg38)NC_000001.11Chr143,699,71343,809,551
    nssv18629181RemappedPerfectNC_000001.10:g.441
    65384_44275222dup
    GRCh37.p13First PassNC_000001.10Chr144,165,38444,275,222

    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)
    nssv186291814e-061275390
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