A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4054n100



Internal ID20155670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114622806..114646501hg38UCSC Ensembl
chr2:115380383..115404078hg19UCSC Ensembl
chr2:115096853..115120548hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3823696
hg1923696
hg1823696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012067, nsv1007559, nsv1000813, nsv1010029, nsv1006645
Samples
Known GenesDPP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4054n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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