A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv26n212



Internal ID22815374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21249564..23111764hg38UCSC Ensembl
chr19:21432366..23294566hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381862201
hg191862201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6044486, nsv6047763
Samples
Known GenesLINC00664, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF492, ZNF493, ZNF676, ZNF708, ZNF728, ZNF729, ZNF738, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)dgv26n212
Frequency
Sample Size405
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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