A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511489



Internal ID288068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40976741..41148369hg38UCSC Ensembl
chr11:40998291..41169919hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38171629
hg19171629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043843
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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