A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524920



Internal ID301102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50329498..50329733hg38UCSC Ensembl
chr16:50363409..50363644hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708966
Samples
Known GenesBRD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524920
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