A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091029



Internal ID20658069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79767547..79770853hg38UCSC Ensembl
chr2:79994673..79997979hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343365
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091029
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