A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880795



Internal ID22655765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94182686..94188702hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1206n209
Supporting Variantsnssv17407957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880795
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