A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4059n100



Internal ID22790146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:117211492..117373492hg38UCSC Ensembl
chr2:117969068..118131068hg19UCSC Ensembl
chr2:117685538..117847538hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38162001
hg19162001
hg18162001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998715, nsv1011331, nsv1006693, nsv1010293
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)dgv4059n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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