A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4222n223



Internal ID22807190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:188317075..188382658hg38UCSC Ensembl
chr2:189181802..189247385hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3865584
hg1965584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6351271, nsv6337890
Samples
Known GenesGULP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4222n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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