A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185904



Internal ID20752944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9340404..9345425hg38UCSC Ensembl
chr11:9361951..9366972hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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