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nsv6852463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,327

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 239 SVs from 34 studies. See in: genome view    
    Submitted genomic17,770,679-17,780,005Question Mark
    Overlapping variant regions from other studies: 239 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):17,628,188-17,637,514Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6852463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,770,67917,780,005
    nsv6852463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,628,18817,637,514

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736172duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736172Submitted genomicNC_000008.11:g.177
    70679_17780005dup
    GRCh38 (hg38)NC_000008.11Chr817,770,67917,780,005
    nssv18736172RemappedPerfectNC_000008.10:g.176
    28188_17637514dup
    GRCh37.p13First PassNC_000008.10Chr817,628,18817,637,514

    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)
    nssv187361721.8e-055274530
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