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nsv6562231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,317,791

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 24865 SVs from 121 studies. See in: genome view    
    Submitted genomic150,783,018-160,100,808Question Mark
    Overlapping variant regions from other studies: 24867 SVs from 121 studies. See in: genome view    
    Remapped(Score: Good):151,104,154-160,521,840Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6562231Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6150,783,018160,100,808
    nsv6562231RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6151,104,154160,521,840

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18269338inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18269338Submitted genomicNC_000006.12:g.150
    783018_160100808in
    v
    GRCh38 (hg38)NC_000006.12Chr6150,783,018160,100,808
    nssv18269338RemappedGoodNC_000006.11:g.151
    104154_160521840in
    v
    GRCh37.p13First PassNC_000006.11Chr6151,104,154160,521,840

    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)
    nssv18269338<0.0011835894
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