A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463037



Internal ID22520922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:263982..280711hg38UCSC Ensembl
chr11:263982..280711hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816730
hg1916730
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867415
Supporting Variants
Samples
Known GenesNLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463037
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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