A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921168



Internal ID22696391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:263081..280481hg38UCSC Ensembl
chr11:263081..280481hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3817401
hg1917401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367796
Samples
Known GenesNLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921168
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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