A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004399



Internal ID22066030
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154336
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004399
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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