A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154336



Internal ID22084841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33645011..33670356hg38UCSC Ensembl
Outerchr8:33640133..33674608hg38UCSC Ensembl
Innerchr8:33502529..33527874hg19UCSC Ensembl
Outerchr8:33497651..33532126hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3834476
hg1934476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004399
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154336
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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