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nsv7054437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,369

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 31 studies. See in: genome view    
    Submitted genomic101,858,545-101,862,913Question Mark
    Overlapping variant regions from other studies: 163 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):102,324,101-102,328,469Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,858,545101,862,913
    nsv7054437RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,324,101102,328,469

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742698inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742698Submitted genomicNC_000001.11:g.101
    858545_101862913in
    v
    GRCh38 (hg38)NC_000001.11Chr1101,858,545101,862,913
    nssv18742698RemappedPerfectNC_000001.10:g.102
    324101_102328469in
    v
    GRCh37.p13First PassNC_000001.10Chr1102,324,101102,328,469

    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)
    nssv187426984e-061276268
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