A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1162n100



Internal ID22787249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54953335..55268984hg38UCSC Ensembl
chr11:54720811..55036460hg19UCSC Ensembl
chr11:54477387..54793036hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38315650
hg19315650
hg18315650
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047352, nsv1043891, nsv1039476
Samples
Known GenesTRIM48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1162n100
Frequency
Sample Size11257
Observed Gain32
Observed Loss6
Observed Complex0
Frequencyn/a


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