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nsv6797587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
    Submitted genomic49,737,993-49,738,124Question Mark
    Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):49,705,706-49,705,837Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6797587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,737,99349,738,124
    nsv6797587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,705,70649,705,837

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715911duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715911Submitted genomicNC_000006.12:g.497
    37993_49738124dup
    GRCh38 (hg38)NC_000006.12Chr649,737,99349,738,124
    nssv18715911RemappedPerfectNC_000006.11:g.497
    05706_49705837dup
    GRCh37.p13First PassNC_000006.11Chr649,705,70649,705,837

    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)
    nssv187159115.2e-0512225306
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