A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154919



Internal ID22085424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63727471..63754959hg38UCSC Ensembl
Outerchr13:63715183..63770336hg38UCSC Ensembl
Innerchr13:64301604..64329092hg19UCSC Ensembl
Outerchr13:64289316..64344469hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3855154
hg1955154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008155
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154919
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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