A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801944



Internal ID15749214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109702385..109714969hg38UCSC Ensembl
Innerchr12:110140190..110152774hg19UCSC Ensembl
Innerchr12:108624573..108637157hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3812585
hg1912585
hg1812585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560127
Supporting Variants
Samples
Known GenesFAM222A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801944
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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