A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523875



Internal ID300093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52142537..52142587hg38UCSC Ensembl
chr15:52434734..52434784hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702746
Samples
Known GenesGNB5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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