A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1319n100



Internal ID22787406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134948674..135074876hg38UCSC Ensembl
chr11:134818568..134944770hg19UCSC Ensembl
chr11:134323778..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38126203
hg19126203
hg18126205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046747, nsv1052345, nsv1053058, nsv1040207
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)dgv1319n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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