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nsv6916580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:179,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1476 SVs from 84 studies. See in: genome view    
    Submitted genomic385,701-565,300Question Mark
    Overlapping variant regions from other studies: 1476 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):494,867-674,466Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6916580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12385,701565,300
    nsv6916580RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12494,867674,466

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596505duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596505Submitted genomicNC_000012.12:g.385
    701_565300dup
    GRCh38 (hg38)NC_000012.12Chr12385,701565,300
    nssv18596505RemappedPerfectNC_000012.11:g.494
    867_674466dup
    GRCh37.p13First PassNC_000012.11Chr12494,867674,466

    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)
    nssv185965054e-061275758
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