A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1623n223



Internal ID22804591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78613434..78629273hg38UCSC Ensembl
chr12:79007214..79023053hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3815840
hg1915840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6471533, nsv6468042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1623n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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