A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3758n100



Internal ID22789845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34423619..34529892hg38UCSC Ensembl
chr2:34648686..34754959hg19UCSC Ensembl
chr2:34502190..34608463hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38106274
hg19106274
hg18106274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011574, nsv1005928, nsv998181, nsv1005072, nsv1000385, nsv1005267, nsv1007715, nsv1009862, nsv1009475, nsv1013812, nsv998133, nsv1013661, nsv1013924, nsv997997
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)dgv3758n100
Frequency
Sample Size11257
Observed Gain80
Observed Loss0
Observed Complex0
Frequencyn/a


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