A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4635n100



Internal ID20156251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2221008..2299059hg38UCSC Ensembl
chr3:2262692..2340743hg19UCSC Ensembl
chr3:2237692..2315743hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3878052
hg1978052
hg1878052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008972, nsv1001161
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4635n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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