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nsv6856903

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,863

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 305 SVs from 40 studies. See in: genome view    
    Submitted genomic11,500,355-11,528,217Question Mark
    Overlapping variant regions from other studies: 305 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):11,357,864-11,385,726Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6856903Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,500,35511,528,217
    nsv6856903RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,357,86411,385,726

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18730550duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18730550Submitted genomicNC_000008.11:g.115
    00355_11528217dup
    GRCh38 (hg38)NC_000008.11Chr811,500,35511,528,217
    nssv18730550RemappedPerfectNC_000008.10:g.113
    57864_11385726dup
    GRCh37.p13First PassNC_000008.10Chr811,357,86411,385,726

    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)
    nssv187305501.4e-054275878
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