A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1223n100



Internal ID22787310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71641081..71827945hg38UCSC Ensembl
chr11:71352127..71538991hg19UCSC Ensembl
chr11:71029775..71216639hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38186865
hg19186865
hg18186865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047177, nsv1044072, nsv1047568, nsv1054575, nsv1049480, nsv1038551
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1223n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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