nsv7061496

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:572,328

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1295 SVs from 75 studies. See in: genome view    
    Submitted genomic110,868,674-111,441,001Question Mark
    Overlapping variant regions from other studies: 1295 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):111,306,478-111,878,805Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061496Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12110,868,674111,441,001
    nsv7061496RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12111,306,478111,878,805

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751607inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751607Submitted genomicNC_000012.12:g.110
    868674_111441001in
    v
    GRCh38 (hg38)NC_000012.12Chr12110,868,674111,441,001
    nssv18751607RemappedPerfectNC_000012.11:g.111
    306478_111878805in
    v
    GRCh37.p13First PassNC_000012.11Chr12111,306,478111,878,805

    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)
    nssv187516074e-061276268
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