A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091094



Internal ID20658134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80532763..80533576hg38UCSC Ensembl
chr2:80759888..80760701hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345579
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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