A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1303n223



Internal ID22804271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107589747..108069600hg38UCSC Ensembl
chr11:107460473..107940327hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38479854
hg19479855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6456840, nsv6460245
Samples
Known GenesCUL5, ELMOD1, LOC643923, RAB39A, SLC35F2, SLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1303n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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