A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449231



Internal ID227474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174448773..174452886hg38UCSC Ensembl
chr2:175313501..175317614hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921089
Samples
Known GenesGPR155
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449231
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