A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2336n54



Internal ID22770231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7869336..7938243hg38UCSC Ensembl
chr12:8021932..8090839hg19UCSC Ensembl
chr12:7913199..7982106hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3868908
hg1968908
hg1868908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv557324, nsv557321, nsv557323, nsv557322
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2336n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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