A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009866



Internal ID18752397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114186492..114251552hg38UCSC Ensembl
Innerchr3:113905339..113970399hg19UCSC Ensembl
Innerchr3:115388029..115453089hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3865061
hg1965061
hg1865061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604465
Samples
Known GenesDRD3, ZNF80
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009866
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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