A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186182



Internal ID20753222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86289529..86297096hg38UCSC Ensembl
chr11:86000571..86008138hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg387568
hg197568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465878
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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