A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1265n100



Internal ID20152881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100017658..100758405hg38UCSC Ensembl
chr11:99888390..100629136hg19UCSC Ensembl
chr11:99393600..100134346hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38740748
hg19740747
hg18740747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037689, nsv1040942, nsv1053430, nsv1042067
Samples
Known GenesARHGAP42, CNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1265n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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