A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1235n100



Internal ID22787322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78309406..78374607hg38UCSC Ensembl
chr11:78020452..78085653hg19UCSC Ensembl
chr11:77698100..77763301hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3865202
hg1965202
hg1865202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052165, nsv1049483
Samples
Known GenesGAB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1235n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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