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nsv7038576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,257,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3645 SVs from 108 studies. See in: genome view    
    Submitted genomic16,300,700-17,558,371Question Mark
    Overlapping variant regions from other studies: 3645 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):16,340,325-17,597,995Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,300,70017,558,371
    nsv7038576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,340,32517,597,995

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781850inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781850Submitted genomicNC_000007.14:g.163
    00700_17558371inv
    GRCh38 (hg38)NC_000007.14Chr716,300,70017,558,371
    nssv18781850RemappedPerfectNC_000007.13:g.163
    40325_17597995inv
    GRCh37.p13First PassNC_000007.13Chr716,340,32517,597,995

    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)
    nssv187818504e-061276268
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