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nsv6875760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 390 SVs from 47 studies. See in: genome view    
    Submitted genomic5,135,401-5,145,500Question Mark
    Overlapping variant regions from other studies: 392 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):5,135,401-5,145,500Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr95,135,4015,145,500
    nsv6875760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr95,135,4015,145,500

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745917duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745917Submitted genomicNC_000009.12:g.513
    5401_5145500dup
    GRCh38 (hg38)NC_000009.12Chr95,135,4015,145,500
    nssv18745917RemappedPerfectNC_000009.11:g.513
    5401_5145500dup
    GRCh37.p13First PassNC_000009.11Chr95,135,4015,145,500

    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)
    nssv18745917<0.00182265256
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