A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155652



Internal ID22086157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24910309..24945082hg38UCSC Ensembl
Outerchr20:24908439..24950006hg38UCSC Ensembl
Innerchr20:24890945..24925718hg19UCSC Ensembl
Outerchr20:24889075..24930642hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3841568
hg1941568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013884
Samples
Known GenesCST7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155652
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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