A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4946n223



Internal ID22807914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95742301..95770700hg38UCSC Ensembl
chr3:95461145..95489544hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3828400
hg1928400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6363598, nsv6358975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4946n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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