nsv6397224

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,370

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 44 studies. See in: genome view    
    Submitted genomic115,902,990-115,913,359Question Mark
    Overlapping variant regions from other studies: 181 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):115,238,687-115,249,056Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6397224Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,902,990115,913,359
    nsv6397224RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,238,687115,249,056

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125653deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125653Submitted genomicNC_000005.10:g.115
    902990_115913359de
    l
    GRCh38 (hg38)NC_000005.10Chr5115,902,990115,913,359
    nssv18125653RemappedPerfectNC_000005.9:g.1152
    38687_115249056del
    GRCh37.p13First PassNC_000005.9Chr5115,238,687115,249,056

    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)
    nssv18125653<0.001325612
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