A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701113



Internal ID124779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41286874..41292874hg38UCSC Ensembl
chr15:41579072..41585072hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511975
Supporting Variants
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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