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nsv6888094

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 23 studies. See in: genome view    
    Submitted genomic18,656,701-18,665,700Question Mark
    Overlapping variant regions from other studies: 96 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):18,945,630-18,954,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6888094Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1018,656,70118,665,700
    nsv6888094RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1018,945,63018,954,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573503duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573503Submitted genomicNC_000010.11:g.186
    56701_18665700dup
    GRCh38 (hg38)NC_000010.11Chr1018,656,70118,665,700
    nssv18573503RemappedPerfectNC_000010.10:g.189
    45630_18954629dup
    GRCh37.p13First PassNC_000010.10Chr1018,945,63018,954,629

    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)
    nssv185735034e-061275270
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