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nsv6902306

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,771

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 63 SVs from 21 studies. See in: genome view    
    Submitted genomic7,063,035-7,068,805Question Mark
    Overlapping variant regions from other studies: 63 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):7,084,266-7,090,036Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6902306Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr117,063,0357,068,805
    nsv6902306RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr117,084,2667,090,036

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353234deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353234Submitted genomicNC_000011.10:g.706
    3035_7068805del
    GRCh38 (hg38)NC_000011.10Chr117,063,0357,068,805
    nssv18353234RemappedPerfectNC_000011.9:g.7084
    266_7090036del
    GRCh37.p13First PassNC_000011.9Chr117,084,2667,090,036

    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)
    nssv183532341.8e-055275610
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