A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv986n223



Internal ID22803954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21332744..21359207hg38UCSC Ensembl
chr11:21354290..21380753hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3826464
hg1926464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6449562, nsv6438300
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv986n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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