A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155763



Internal ID22086268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15533086..15602991hg38UCSC Ensembl
Outerchr22:15500909..15612468hg38UCSC Ensembl
Innerchr22:16374972..16444877hg19UCSC Ensembl
Outerchr22:16365495..16477054hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38111560
hg19111560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015006
Samples
Known GenesOR11H1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155763
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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