A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143777



Internal ID342978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2898000..2908000hg38UCSC Ensembl
chr11:2919230..2929230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042121
Samples
Known GenesSLC22A18, SLC22A18AS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143777
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer