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nsv6548314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:855,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2282 SVs from 85 studies. See in: genome view    
    Submitted genomic177,986,552-178,841,553Question Mark
    Overlapping variant regions from other studies: 2282 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):178,851,279-179,706,280Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6548314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2177,986,552178,841,553
    nsv6548314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2178,851,279179,706,280

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256226inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256226Submitted genomicNC_000002.12:g.177
    986552_178841553in
    v
    GRCh38 (hg38)NC_000002.12Chr2177,986,552178,841,553
    nssv18256226RemappedPerfectNC_000002.11:g.178
    851279_179706280in
    v
    GRCh37.p13First PassNC_000002.11Chr2178,851,279179,706,280

    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)
    nssv18256226<0.001139304
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