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nsv6548079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,512,291

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21623 SVs from 130 studies. See in: genome view    
    Submitted genomic178,157,654-187,669,944Question Mark
    Overlapping variant regions from other studies: 21624 SVs from 130 studies. See in: genome view    
    Remapped(Score: Perfect):179,022,381-188,534,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6548079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2178,157,654187,669,944
    nsv6548079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2179,022,381188,534,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256291inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256291Submitted genomicNC_000002.12:g.178
    157654_187669944in
    v
    GRCh38 (hg38)NC_000002.12Chr2178,157,654187,669,944
    nssv18256291RemappedPerfectNC_000002.11:g.179
    022381_188534671in
    v
    GRCh37.p13First PassNC_000002.11Chr2179,022,381188,534,671

    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)
    nssv18256291<0.001139304
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