A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155397



Internal ID22085902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31645750..31661534hg38UCSC Ensembl
Outerchr17:31642435..31665332hg38UCSC Ensembl
Innerchr17:29972769..29988553hg19UCSC Ensembl
Outerchr17:29969454..29992351hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3822898
hg1922898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010181
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155397
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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