A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155212



Internal ID22085717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94167111..94212568hg38UCSC Ensembl
Outerchr15:94162693..94213504hg38UCSC Ensembl
Innerchr15:94710340..94755797hg19UCSC Ensembl
Outerchr15:94705922..94756733hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3850812
hg1950812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012186
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155212
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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