A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091096



Internal ID20658136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80549489..80552912hg38UCSC Ensembl
chr2:80776614..80780037hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383424
hg193424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352930
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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