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nsv6397059

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,434

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Submitted genomic148,209,007-148,210,440Question Mark
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):147,588,570-147,590,003Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6397059Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,209,007148,210,440
    nsv6397059RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,588,570147,590,003

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125917deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125917Submitted genomicNC_000005.10:g.148
    209007_148210440de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,209,007148,210,440
    nssv18125917RemappedPerfectNC_000005.9:g.1475
    88570_147590003del
    GRCh37.p13First PassNC_000005.9Chr5147,588,570147,590,003

    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)
    nssv18125917<0.001231066
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