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nsv6839415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:936

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Submitted genomic30,605,338-30,606,273Question Mark
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):30,462,855-30,463,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6839415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr830,605,33830,606,273
    nsv6839415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr830,462,85530,463,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744266duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744266Submitted genomicNC_000008.11:g.306
    05338_30606273dup
    GRCh38 (hg38)NC_000008.11Chr830,605,33830,606,273
    nssv18744266RemappedPerfectNC_000008.10:g.304
    62855_30463790dup
    GRCh37.p13First PassNC_000008.10Chr830,462,85530,463,790

    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)
    nssv187442664e-061262714
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