A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4710n100



Internal ID22790797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26490122..26560273hg38UCSC Ensembl
chr3:26531613..26601764hg19UCSC Ensembl
chr3:26506617..26576768hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3870152
hg1970152
hg1870152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006253, nsv1008029, nsv1013239, nsv997858, nsv1000903
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)dgv4710n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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