A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3739n100



Internal ID22789826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20149582..20193796hg38UCSC Ensembl
chr2:20349343..20393557hg19UCSC Ensembl
chr2:20212824..20257038hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3844215
hg1944215
hg1844215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005524, nsv1001531, nsv998067, nsv997958, nsv1007926
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)dgv3739n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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