A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511129



Internal ID287725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106061833..106062044hg38UCSC Ensembl
chr11:105932560..105932771hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051394
Samples
Known GenesKBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511129
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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