A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529882



Internal ID305885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88475544..88482191hg38UCSC Ensembl
chr15:89018775..89025422hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705519
Samples
Known GenesMRPS11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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