A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1077n100



Internal ID22787164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25102193..25275435hg38UCSC Ensembl
chr11:25123739..25296981hg19UCSC Ensembl
chr11:25080315..25253557hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38173243
hg19173243
hg18173243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038643, nsv1046479, nsv1049506, nsv1038401, nsv1038088
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)dgv1077n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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