A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1337n223



Internal ID22804305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130563109..131215048hg38UCSC Ensembl
chr11:130433004..131084943hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38651940
hg19651940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6467171, nsv6462284
Samples
Known GenesC11orf44, MIR8052, SNX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1337n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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