A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3751n100



Internal ID20155367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32621236..32817450hg38UCSC Ensembl
chr2:32846303..33042517hg19UCSC Ensembl
chr2:32699807..32896021hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38196215
hg19196215
hg18196215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013455, nsv1005305
Samples
Known GenesMIR4765, TTC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3751n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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