A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185061



Internal ID20752101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33110371..33461460hg38UCSC Ensembl
chr11:33131917..33483006hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38351090
hg19351090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456989
Supporting Variants
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185061
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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