A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3831n223



Internal ID22806799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33903788..33986067hg38UCSC Ensembl
chr2:34128855..34211134hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3882280
hg1982280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6351527, nsv6345576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3831n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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