A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3803n100



Internal ID22789890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45103892..45126291hg38UCSC Ensembl
chr2:45331031..45353430hg19UCSC Ensembl
chr2:45184535..45206934hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3822400
hg1922400
hg1822400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013106, nsv1013709, nsv1010563, nsv997810, nsv1003879, nsv1002403, nsv1000942, nsv1009753, nsv1006369
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)dgv3803n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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