A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515625



Internal ID292106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69211161..69229875hg38UCSC Ensembl
chr15:69503500..69522214hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3818715
hg1918715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703946
Samples
Known GenesGLCE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515625
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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