A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143633



Internal ID342834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119070364..119076364hg38UCSC Ensembl
chr11:118941074..118947074hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052226
Samples
Known GenesVPS11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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