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nsv6752530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:542

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Submitted genomic71,490,249-71,490,790Question Mark
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):72,355,966-72,356,507Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr471,490,24971,490,790
    nsv6752530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr472,355,96672,356,507

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18695262duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18695262Submitted genomicNC_000004.12:g.714
    90249_71490790dup
    GRCh38 (hg38)NC_000004.12Chr471,490,24971,490,790
    nssv18695262RemappedPerfectNC_000004.11:g.723
    55966_72356507dup
    GRCh37.p13First PassNC_000004.11Chr472,355,96672,356,507

    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)
    nssv186952624e-061247550
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