A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1017n223



Internal ID22803985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32928988..33107112hg38UCSC Ensembl
chr11:32950534..33128658hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38178125
hg19178125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6472173, nsv6456008
Samples
Known GenesCSTF3, DEPDC7, LINC00294, QSER1, TCP11L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1017n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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