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nsv6885471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,785,334

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3901 SVs from 103 studies. See in: genome view    
    Submitted genomic48,691,383-50,476,716Question Mark
    Overlapping variant regions from other studies: 4438 SVs from 106 studies. See in: genome view    
    Remapped(Score: Pass):49,899,428-52,236,476Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6885471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1048,691,38350,476,716
    nsv6885471RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1049,899,42852,236,476

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582517duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582517Submitted genomicNC_000010.11:g.486
    91383_50476716dup
    GRCh38 (hg38)NC_000010.11Chr1048,691,38350,476,716
    nssv18582517RemappedPassNC_000010.10:g.498
    99428_52236476dup
    GRCh37.p13First PassNC_000010.10Chr1049,899,42852,236,476

    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)
    nssv185825174e-061275304
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