A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915755



Internal ID11236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79535594..79546205hg38UCSC Ensembl
chr2:79762720..79773331hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3810612
hg1910612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443613
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915755
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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