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nsv6581943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,052,393

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2757 SVs from 91 studies. See in: genome view    
    Submitted genomic25,014,412-26,066,804Question Mark
    Overlapping variant regions from other studies: 2759 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):25,588,550-26,640,942Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6581943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1325,014,41226,066,804
    nsv6581943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1325,588,55026,640,942

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18232647inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18232647Submitted genomicNC_000013.11:g.250
    14412_26066804inv
    GRCh38 (hg38)NC_000013.11Chr1325,014,41226,066,804
    nssv18232647RemappedPerfectNC_000013.10:g.255
    88550_26640942inv
    GRCh37.p13First PassNC_000013.10Chr1325,588,55026,640,942

    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)
    nssv18232647<0.0012338982
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