A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495556



Internal ID272665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26671309..26671399hg38UCSC Ensembl
chr15:26916456..26916546hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699556
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495556
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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