A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3807n223



Internal ID22806775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22097798..22212405hg38UCSC Ensembl
chr2:22320670..22435277hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38114608
hg19114608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6335754, nsv6350978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3807n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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