A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4696n100



Internal ID20156312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21942872..21981431hg38UCSC Ensembl
chr3:21984364..22022923hg19UCSC Ensembl
chr3:21959368..21997927hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3838560
hg1938560
hg1838560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009404, nsv1007663, nsv1001030, nsv1007886
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)dgv4696n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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