A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533038



Internal ID308936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63087669..63253345hg38UCSC Ensembl
chr15:63379868..63545544hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38165677
hg19165677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702853
Samples
Known GenesLACTB, RAB8B, RPS27L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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