A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143486



Internal ID342687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90040896..90090896hg38UCSC Ensembl
chr11:89774064..89824064hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850001
hg1950001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv86n206
Supporting Variantsnssv17050842
Samples
Known GenesTRIM49C, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143486
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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