A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3719n100



Internal ID22789806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13060017..13121935hg38UCSC Ensembl
chr2:13200142..13262060hg19UCSC Ensembl
chr2:13117593..13179511hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3861919
hg1961919
hg1861919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009351, nsv1008534, nsv1005070
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)dgv3719n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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