A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3836n223



Internal ID22806804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37906601..37993200hg38UCSC Ensembl
chr2:38133744..38220343hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3886600
hg1986600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6354296, nsv6347953
Samples
Known GenesRMDN2, RMDN2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3836n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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