A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155760



Internal ID22086265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15533086..15925481hg38UCSC Ensembl
Outerchr22:15500909..15925481hg38UCSC Ensembl
Innerchr22:16052528..16444877hg19UCSC Ensembl
Outerchr22:16052528..16477054hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38424573
hg19424527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015004
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155760
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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