A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5015n223



Internal ID22807983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128690001..128696900hg38UCSC Ensembl
chr3:128408844..128415743hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6355759, nsv6375315, nsv6361272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5015n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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