A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1320n100



Internal ID22787407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134973916..135074876hg38UCSC Ensembl
chr11:134843810..134944770hg19UCSC Ensembl
chr11:134349020..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38100961
hg19100961
hg18100963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044102, nsv1037631, nsv1053896, nsv1049414, nsv1050066, nsv1049782, nsv1043934
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)dgv1320n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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