A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3816n100



Internal ID22789903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51856772..52038525hg38UCSC Ensembl
chr2:52083910..52265663hg19UCSC Ensembl
chr2:51937414..52119167hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38181754
hg19181754
hg18181754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004603, nsv999607, nsv1013892
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)dgv3816n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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