A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1279n223



Internal ID22804247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95064501..95072000hg38UCSC Ensembl
chr11:94797665..94805164hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6468916, nsv6456993
Samples
Known GenesSRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1279n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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