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nsv6414572

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,224

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 25 studies. See in: genome view    
    Submitted genomic150,374,196-150,438,419Question Mark
    Overlapping variant regions from other studies: 198 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):149,753,759-149,817,982Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6414572Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5150,374,196150,438,419
    nsv6414572RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5149,753,759149,817,982

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18213286duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18213286Submitted genomicNC_000005.10:g.150
    374196_150438419du
    p
    GRCh38 (hg38)NC_000005.10Chr5150,374,196150,438,419
    nssv18213286RemappedPerfectNC_000005.9:g.1497
    53759_149817982dup
    GRCh37.p13First PassNC_000005.9Chr5149,753,759149,817,982

    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)
    nssv18213286<0.001139294
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