A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4189n54



Internal ID22772084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20359322..20420780hg38UCSC Ensembl
chr15:20564575..20626033hg19UCSC Ensembl
chr15:18824589..18886047hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3861459
hg1961459
hg1861459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567366, nsv567368, nsv567358, nsv567364, nsv567344, nsv567369, nsv567362, nsv567346, nsv567363
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4189n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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