A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1392n223



Internal ID22804360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8786501..8795800hg38UCSC Ensembl
chr12:8939097..8948396hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6459610, nsv6465914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1392n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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