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nsv6642574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101,331

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 339 SVs from 46 studies. See in: genome view    
    Submitted genomic157,941,205-158,042,535Question Mark
    Overlapping variant regions from other studies: 343 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):157,910,995-158,012,325Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1157,941,205158,042,535
    nsv6642574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1157,910,995158,012,325

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18580412duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18580412Submitted genomicNC_000001.11:g.157
    941205_158042535du
    p
    GRCh38 (hg38)NC_000001.11Chr1157,941,205158,042,535
    nssv18580412RemappedPerfectNC_000001.10:g.157
    910995_158012325du
    p
    GRCh37.p13First PassNC_000001.10Chr1157,910,995158,012,325

    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)
    nssv185804122.1e-056275704
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