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nsv7031630

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:430,985

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1755 SVs from 81 studies. See in: genome view    
    Submitted genomic44,430,030-44,861,014Question Mark
    Overlapping variant regions from other studies: 1755 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):44,825,910-45,256,894Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7031630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2244,430,03044,861,014
    nsv7031630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2244,825,91045,256,894

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652592duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652592Submitted genomicNC_000022.11:g.444
    30030_44861014dup
    GRCh38 (hg38)NC_000022.11Chr2244,430,03044,861,014
    nssv18652592RemappedPerfectNC_000022.10:g.448
    25910_45256894dup
    GRCh37.p13First PassNC_000022.10Chr2244,825,91045,256,894

    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)
    nssv186525924e-061275926
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