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nsv6341460

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:571

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 17 studies. See in: genome view    
    Submitted genomic207,213,263-207,213,833Question Mark
    Overlapping variant regions from other studies: 106 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):208,077,987-208,078,557Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6341460Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2207,213,263207,213,833
    nsv6341460RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2208,077,987208,078,557

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18082571deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18082571Submitted genomicNC_000002.12:g.207
    213263_207213833de
    l
    GRCh38 (hg38)NC_000002.12Chr2207,213,263207,213,833
    nssv18082571RemappedPerfectNC_000002.11:g.208
    077987_208078557de
    l
    GRCh37.p13First PassNC_000002.11Chr2208,077,987208,078,557

    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)
    nssv18082571<0.0012238232
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