A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178863



Internal ID20745903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87768508..87825583hg38UCSC Ensembl
chr11:87479400..87536475hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3857076
hg1957076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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