A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852287



Internal ID16146243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3880210..3883093hg38UCSC Ensembl
Innerchr16:3930211..3933094hg19UCSC Ensembl
Innerchr16:3870212..3873095hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382884
hg192884
hg182884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571268
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)nssv852287
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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