A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3738n100



Internal ID22789825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20136476..20188377hg38UCSC Ensembl
chr2:20336237..20388138hg19UCSC Ensembl
chr2:20199718..20251619hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3851902
hg1951902
hg1851902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004083, nsv1004947
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)dgv3738n100
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