A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4532n54



Internal ID22772427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53682798..53684200hg38UCSC Ensembl
chr15:53974995..53976397hg19UCSC Ensembl
chr15:51762287..51763689hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381403
hg191403
hg181403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569447, nsv569446
Samples
Known GenesWDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4532n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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