A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180070



Internal ID20747110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134893174..135060158hg38UCSC Ensembl
chr11:134763068..134930052hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38166985
hg19166985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180070
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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