A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv191e55



Internal ID22761141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160874284..161016270hg38UCSC Ensembl
chr4:161795436..161937422hg19UCSC Ensembl
chr4:162014886..162156872hg18UCSC Ensembl
chr4:162153041..162295027hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38141987
hg19141987
hg18141987
hg17141987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34806, esv34413
SamplesNA18947, NA18633
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv191e55
Frequency
Sample Size771
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer