A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010487



Internal ID22072118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9725329..9736279hg38UCSC Ensembl
Outerchr16:9725192..9737174hg38UCSC Ensembl
Innerchr16:9819186..9830136hg19UCSC Ensembl
Outerchr16:9819049..9831031hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3811983
hg1911983
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155229
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010487
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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