A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196005



Internal ID20763045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65928668..65939393hg38UCSC Ensembl
chr11:65696139..65706864hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810726
hg1910726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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