A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889699



Internal ID22664719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22446924..22448282hg38UCSC Ensembl
chr4:22448547..22449905hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409641
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889699
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