A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436819



Internal ID215426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28421551..28431244hg38UCSC Ensembl
chr3:28463042..28472735hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg389694
hg199694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930772
Samples
Known GenesZCWPW2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436819
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