A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1198n223



Internal ID22804166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59137701..59183100hg38UCSC Ensembl
chr11:58905174..58950573hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3845400
hg1945400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6457560, nsv6462772
Samples
Known GenesDTX4, FAM111A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1198n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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