A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3761n100



Internal ID22789848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34450388..34517957hg38UCSC Ensembl
chr2:34675455..34743024hg19UCSC Ensembl
chr2:34528959..34596528hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3867570
hg1967570
hg1867570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010024, nsv1008155, nsv1010755, nsv1008385, nsv1001568, nsv1007221, nsv999193, nsv1012304, nsv1005316, nsv1008096, nsv1010856, nsv997456, nsv1008782, nsv998779, nsv1007054, nsv1004770, nsv1006035, nsv998386, nsv1002314, nsv1008709, nsv999954, nsv1002999, nsv1007630
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)dgv3761n100
Frequency
Sample Size11257
Observed Gain70
Observed Loss0
Observed Complex0
Frequencyn/a


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