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nsv6671434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:364,795

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 980 SVs from 78 studies. See in: genome view    
    Submitted genomic64,150,059-64,514,853Question Mark
    Overlapping variant regions from other studies: 980 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):64,377,193-64,741,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6671434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr264,150,05964,514,853
    nsv6671434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr264,377,19364,741,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666112duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666112Submitted genomicNC_000002.12:g.641
    50059_64514853dup
    GRCh38 (hg38)NC_000002.12Chr264,150,05964,514,853
    nssv18666112RemappedPerfectNC_000002.11:g.643
    77193_64741987dup
    GRCh37.p13First PassNC_000002.11Chr264,377,19364,741,987

    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)
    nssv186661124e-061275460
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