A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4695n100



Internal ID22790782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21934529..21959454hg38UCSC Ensembl
chr3:21976021..22000946hg19UCSC Ensembl
chr3:21951025..21975950hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3824926
hg1924926
hg1824926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012217, nsv1012736
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)dgv4695n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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