A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1232n223



Internal ID22804200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76960701..76966100hg38UCSC Ensembl
chr11:76671745..76677144hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6473647, nsv6461535
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1232n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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