A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517824



Internal ID294231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53684874..53693600hg38UCSC Ensembl
chr15:53977071..53985797hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg388727
hg198727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701249
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517824
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