A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012131



Internal ID22073762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80230629..80234268hg38UCSC Ensembl
Outerchr15:80227841..80238172hg38UCSC Ensembl
Innerchr15:80522971..80526610hg19UCSC Ensembl
Outerchr15:80520183..80530514hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3810332
hg1910332
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155200
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012131
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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