A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518492



Internal ID21842851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135355486..135357414hg38UCSC Ensembl
chr2:136113056..136114984hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986422
Supporting Variants
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518492
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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