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nsv6782047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:164

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic49,731,514-49,731,677Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):49,699,227-49,699,390Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6782047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,731,51449,731,677
    nsv6782047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,699,22749,699,390

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715910duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715910Submitted genomicNC_000006.12:g.497
    31514_49731677dup
    GRCh38 (hg38)NC_000006.12Chr649,731,51449,731,677
    nssv18715910RemappedPerfectNC_000006.11:g.496
    99227_49699390dup
    GRCh37.p13First PassNC_000006.11Chr649,699,22749,699,390

    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)
    nssv187159106.5e-0515224288
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