A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3948n223



Internal ID22806916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83514850..83868791hg38UCSC Ensembl
chr2:83741974..84095915hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38353942
hg19353942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6336208, nsv6346527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3948n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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