A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509012



Internal ID285682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90471866..90611535hg38UCSC Ensembl
chr11:90205034..90344703hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38139670
hg19139670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050914
Samples
Known GenesDISC1FP1, MIR4490
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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