A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155200



Internal ID22085705
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 TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012133, nssv4012131, nssv4012132
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155200
Frequency
Sample Size131
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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