A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5026n223



Internal ID22807994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132998701..133006200hg38UCSC Ensembl
chr3:132717545..132725044hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6368443, nsv6356033, nsv6362045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5026n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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