A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498253



Internal ID275250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36907124..37638725hg38UCSC Ensembl
chr15:37199325..37930926hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38731602
hg19731602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701974
Samples
Known GenesMEIS2, MIR8063
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498253
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer