A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569445



Internal ID16356854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53682370..53693253hg38UCSC Ensembl
Innerchr15:53974567..53985450hg19UCSC Ensembl
Innerchr15:51761859..51772742hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810884
hg1910884
hg1810884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843036
Samples
Known GenesWDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569445
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