A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv230n209



Internal ID22826305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44607997..44611181hg38UCSC Ensembl
chr11:44629547..44632731hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383185
hg193185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5912175, nsv5918291
Samples
Known GenesCD82
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv230n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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