A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4629n100



Internal ID20156245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1801319..2838526hg38UCSC Ensembl
chr3:1843003..2880210hg19UCSC Ensembl
chr3:1818003..2855210hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg381037208
hg191037208
hg181037208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999932, nsv999351
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4629n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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