A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155229



Internal ID22085734
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010487
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155229
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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