A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569446



Internal ID16356855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53682798..53683970hg38UCSC Ensembl
Innerchr15:53974995..53976167hg19UCSC Ensembl
Innerchr15:51762287..51763459hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381173
hg191173
hg181173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4532n54
Supporting Variantsnssv843037
Samples
Known GenesWDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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