A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571302



Internal ID16012025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4708464..4762815hg38UCSC Ensembl
Innerchr16:4758465..4812816hg19UCSC Ensembl
Innerchr16:4698466..4752817hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3854352
hg1954352
hg1854352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852341
Samples
Known GenesANKS3, C16orf71, ZNF500
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571302
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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