A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4687n223



Internal ID22807655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31769799..31770751hg38UCSC Ensembl
chr22:32165785..32166737hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598563, nsv6597075
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4687n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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