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nsv6788632

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 714 SVs from 67 studies. See in: genome view    
    Submitted genomic180,096,401-180,286,200Question Mark
    Overlapping variant regions from other studies: 714 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):179,523,401-179,713,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6788632Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,096,401180,286,200
    nsv6788632RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,523,401179,713,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18702133duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18702133Submitted genomicNC_000005.10:g.180
    096401_180286200du
    p
    GRCh38 (hg38)NC_000005.10Chr5180,096,401180,286,200
    nssv18702133RemappedPerfectNC_000005.9:g.1795
    23401_179713200dup
    GRCh37.p13First PassNC_000005.9Chr5179,523,401179,713,200

    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)
    nssv18702133<0.001121257988
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