A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569432



Internal ID16010155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53493286..53519424hg38UCSC Ensembl
Innerchr15:53785483..53811621hg19UCSC Ensembl
Innerchr15:51572775..51598913hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3826139
hg1926139
hg1826139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843018
Samples
Known GenesWDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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