A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953459



Internal ID36325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102840847..102842990hg38UCSC Ensembl
chr4:103762004..103764147hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461648
Supporting Variants
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953459
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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