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nsv6856639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,325

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 31 studies. See in: genome view    
    Submitted genomic39,278,966-39,289,290Question Mark
    Overlapping variant regions from other studies: 181 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):39,136,485-39,146,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6856639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,278,96639,289,290
    nsv6856639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,136,48539,146,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18556416deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18556416Submitted genomicNC_000008.11:g.392
    78966_39289290del
    GRCh38 (hg38)NC_000008.11Chr839,278,96639,289,290
    nssv18556416RemappedPerfectNC_000008.10:g.391
    36485_39146809del
    GRCh37.p13First PassNC_000008.10Chr839,136,48539,146,809

    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)
    nssv185564164e-060276120
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