A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187068



Internal ID20754108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33089041..33509598hg38UCSC Ensembl
chr11:33110587..33531144hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38420558
hg19420558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461604
Supporting Variants
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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