A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1624n223



Internal ID22804592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78778001..78817400hg38UCSC Ensembl
chr12:79171781..79211180hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3839400
hg1939400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6473752, nsv6457583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1624n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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