A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155559



Internal ID22086064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17972854..17976402hg38UCSC Ensembl
Outerchr19:17966808..17986614hg38UCSC Ensembl
Innerchr19:18083663..18087211hg19UCSC Ensembl
Outerchr19:18077617..18097423hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3819807
hg1919807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013460
Samples
Known GenesKCNN1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155559
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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