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nsv7026600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,283

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 502 SVs from 59 studies. See in: genome view    
    Submitted genomic41,879,894-41,934,176Question Mark
    Overlapping variant regions from other studies: 503 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):43,300,003-43,354,285Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7026600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2141,879,89441,934,176
    nsv7026600RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2143,300,00343,354,285

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644029duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644029Submitted genomicNC_000021.9:g.4187
    9894_41934176dup
    GRCh38 (hg38)NC_000021.9Chr2141,879,89441,934,176
    nssv18644029RemappedPerfectNC_000021.8:g.4330
    0003_43354285dup
    GRCh37.p13First PassNC_000021.8Chr2143,300,00343,354,285

    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)
    nssv186440294e-061274580
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