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nsv6415334

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 35 studies. See in: genome view    
    Submitted genomic148,209,401-148,213,200Question Mark
    Overlapping variant regions from other studies: 134 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):147,588,964-147,592,763Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6415334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,209,401148,213,200
    nsv6415334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,588,964147,592,763

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125918deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125918Submitted genomicNC_000005.10:g.148
    209401_148213200de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,209,401148,213,200
    nssv18125918RemappedPerfectNC_000005.9:g.1475
    88964_147592763del
    GRCh37.p13First PassNC_000005.9Chr5147,588,964147,592,763

    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)
    nssv18125918<0.001133728
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