A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4764n223



Internal ID22807732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3933489..4219482hg38UCSC Ensembl
chr3:3975173..4261166hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38285994
hg19285994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6372083, nsv6373762, nsv6375339, nsv6366033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4764n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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