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nsv7051193

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,012

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 171 SVs from 42 studies. See in: genome view    
    Submitted genomic228,058,986-228,093,997Question Mark
    Overlapping variant regions from other studies: 171 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):228,923,702-228,958,713Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051193Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,058,986228,093,997
    nsv7051193RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,923,702228,958,713

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767674inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767674Submitted genomicNC_000002.12:g.228
    058986_228093997in
    v
    GRCh38 (hg38)NC_000002.12Chr2228,058,986228,093,997
    nssv18767674RemappedPerfectNC_000002.11:g.228
    923702_228958713in
    v
    GRCh37.p13First PassNC_000002.11Chr2228,923,702228,958,713

    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)
    nssv187676741.1e-053273786
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