A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510897



Internal ID287505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47192693..47213550hg38UCSC Ensembl
chr11:47214244..47235101hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3820858
hg1920858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510897
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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