A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510140



Internal ID286769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90674377..90682479hg38UCSC Ensembl
chr11:90407545..90415647hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg388103
hg198103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050936
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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