A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510362



Internal ID286984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94121081..94125311hg38UCSC Ensembl
chr11:93854247..93858477hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384231
hg194231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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