A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1304n100



Internal ID20152920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134322594..134754120hg38UCSC Ensembl
chr11:134192488..134624014hg19UCSC Ensembl
chr11:133697698..134129224hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38431527
hg19431527
hg18431527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037759, nsv1048815
Samples
Known GenesB3GAT1, GLB1L2, LOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1304n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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