A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965525



Internal ID22740460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44674945..44675249hg38UCSC Ensembl
chr22:45070825..45071129hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399106
Samples
Known GenesPRR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965525
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer