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nsv7029975

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:227

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 18 studies. See in: genome view    
    Submitted genomic44,391,734-44,391,960Question Mark
    Overlapping variant regions from other studies: 124 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):43,020,374-43,020,600Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7029975Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,391,73444,391,960
    nsv7029975RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,020,37443,020,600

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642134duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642134Submitted genomicNC_000020.11:g.443
    91734_44391960dup
    GRCh38 (hg38)NC_000020.11Chr2044,391,73444,391,960
    nssv18642134RemappedPerfectNC_000020.10:g.430
    20374_43020600dup
    GRCh37.p13First PassNC_000020.10Chr2043,020,37443,020,600

    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)
    nssv186421345.8e-0513235240
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