A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv85n21



Internal ID18990558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133118684..133134954hg38UCSC Ensembl
chr11:132988579..133004849hg19UCSC Ensembl
chr11:132493789..132510059hg18UCSC Ensembl
chr11:132493789..132510059hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3816271
hg1916271
hg1816271
hg1716271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523117, nsv516629
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv85n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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