A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1391n223



Internal ID22804359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8784901..8795800hg38UCSC Ensembl
chr12:8937497..8948396hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6470298, nsv6469825, nsv6459273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1391n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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