A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1134n100



Internal ID22787221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49990637..50810134hg38UCSC Ensembl
chr11:50012174..50769305hg19UCSC Ensembl
chr11:49968750..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38819498
hg19757132
hg18757132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051800, nsv1036371, nsv1045083, nsv1035727, nsv1051699, nsv1051873, nsv1047235, nsv1042993, nsv1044792, nsv1037403
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1134n100
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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