A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185828



Internal ID20752868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:277180..290570hg38UCSC Ensembl
chr11:277180..290570hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813391
hg1913391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448396
Supporting Variants
Samples
Known GenesATHL1, NLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185828
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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