A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187631



Internal ID20754671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86195589..86218613hg38UCSC Ensembl
chr11:85906631..85929655hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3823025
hg1923025
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187631
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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