A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1339n223



Internal ID22804307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053101..132060600hg38UCSC Ensembl
chr11:131922995..131930494hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6469067, nsv6466961
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1339n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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