A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143526



Internal ID342727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108385232..108396179hg38UCSC Ensembl
chr11:108255959..108266906hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810948
hg1910948
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049125
Samples
Known GenesC11orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143526
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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