A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867415



Internal ID22642350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:263982..280711hg38UCSC Ensembl
chr11:263982..280711hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816730
hg1916730
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463037, nssv17458746
Samples
Known GenesNLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867415
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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