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nsv6987402

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 390 SVs from 50 studies. See in: genome view    
    Submitted genomic59,116,764-59,186,435Question Mark
    Overlapping variant regions from other studies: 389 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):57,194,125-57,263,796Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1759,116,76459,186,435
    nsv6987402RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1757,194,12557,263,796

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627318duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627318Submitted genomicNC_000017.11:g.591
    16764_59186435dup
    GRCh38 (hg38)NC_000017.11Chr1759,116,76459,186,435
    nssv18627318RemappedPerfectNC_000017.10:g.571
    94125_57263796dup
    GRCh37.p13First PassNC_000017.10Chr1757,194,12557,263,796

    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)
    nssv186273184e-061276008
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