A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513834



Internal ID290346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90217659..90310416hg38UCSC Ensembl
chr11:89950827..90043584hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3892758
hg1992758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050877
Samples
Known GenesCHORDC1, DISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513834
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