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nsv7045773

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:197,445

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 674 SVs from 70 studies. See in: genome view    
    Submitted genomic100,499,070-100,696,514Question Mark
    Overlapping variant regions from other studies: 674 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):100,096,693-100,294,137Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045773Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,499,070100,696,514
    nsv7045773RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7100,096,693100,294,137

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780388inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780388Submitted genomicNC_000007.14:g.100
    499070_100696514in
    v
    GRCh38 (hg38)NC_000007.14Chr7100,499,070100,696,514
    nssv18780388RemappedPerfectNC_000007.13:g.100
    096693_100294137in
    v
    GRCh37.p13First PassNC_000007.13Chr7100,096,693100,294,137

    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)
    nssv18780388<0.0016266586
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