A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1094n100



Internal ID19011462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34620051..34772477hg38UCSC Ensembl
chr11:34641598..34794024hg19UCSC Ensembl
chr11:34598174..34750600hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38152427
hg19152427
hg18152427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052008, nsv1051492, nsv1045130, nsv1052192
Samples
Known GenesEHF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1094n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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