A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143871



Internal ID343073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90028500..90092000hg38UCSC Ensembl
chr11:89761668..89825168hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3863501
hg1963501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv86n206
Supporting Variantsnssv17050838
Samples
Known GenesTRIM49C, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143871
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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