A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465226



Internal ID21122779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103052901..103053900hg38UCSC Ensembl
chr11:102923630..102924629hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985519
Samples
Known GenesDCUN1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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