A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435722



Internal ID214356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156784763..156785385hg38UCSC Ensembl
chr3:156502552..156503174hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940051
Samples
Known GenesLINC00886
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435722
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