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nsv7044207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,033

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
    Submitted genomic210,065,405-210,068,437Question Mark
    Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):210,930,129-210,933,161Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044207Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2210,065,405210,068,437
    nsv7044207RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2210,930,129210,933,161

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767651inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767651Submitted genomicNC_000002.12:g.210
    065405_210068437in
    v
    GRCh38 (hg38)NC_000002.12Chr2210,065,405210,068,437
    nssv18767651RemappedPerfectNC_000002.11:g.210
    930129_210933161in
    v
    GRCh37.p13First PassNC_000002.11Chr2210,930,129210,933,161

    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)
    nssv187676514e-061276268
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