A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156840



Internal ID22087241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168119873..168122176hg38UCSC Ensembl
Outerchr1:168113769..168125471hg38UCSC Ensembl
Innerchr1:168089111..168091414hg19UCSC Ensembl
Outerchr1:168083007..168094709hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3811703
hg1911703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022976
Samples
Known GenesGPR161
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156840
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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