A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533443



Internal ID309334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53684874..53690874hg38UCSC Ensembl
chr15:53977071..53983071hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701248
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533443
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