A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181122



Internal ID20748162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8052587..8066390hg38UCSC Ensembl
chr11:8074134..8087937hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3813804
hg1913804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441562
Supporting Variants
Samples
Known GenesTUB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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