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nsv6644458

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,575

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 29 studies. See in: genome view    
    Submitted genomic171,284,322-171,285,896Question Mark
    Overlapping variant regions from other studies: 172 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):171,253,461-171,255,035Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644458Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,284,322171,285,896
    nsv6644458RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,253,461171,255,035

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18578480duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18578480Submitted genomicNC_000001.11:g.171
    284322_171285896du
    p
    GRCh38 (hg38)NC_000001.11Chr1171,284,322171,285,896
    nssv18578480RemappedPerfectNC_000001.10:g.171
    253461_171255035du
    p
    GRCh37.p13First PassNC_000001.10Chr1171,253,461171,255,035

    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)
    nssv185784802.6e-057266982
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