A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1101n100



Internal ID22787188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37746263..37839444hg38UCSC Ensembl
chr11:37767813..37860994hg19UCSC Ensembl
chr11:37724389..37817570hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3893182
hg1993182
hg1893182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040071, nsv1041813, nsv1051107, nsv1038840, nsv1050878
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1101n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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