A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012186



Internal ID22073817
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155212
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012186
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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