A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881266



Internal ID22656241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80292378..80292540hg38UCSC Ensembl
chr2:80519503..80519665hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394798
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881266
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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