A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852332



Internal ID16146288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315622..4316990hg38UCSC Ensembl
Innerchr16:4365623..4366991hg19UCSC Ensembl
Innerchr16:4305624..4306992hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381369
hg191369
hg181369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571296
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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