A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196658



Internal ID20763698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86421744..86451694hg38UCSC Ensembl
chr11:86132786..86162736hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3829951
hg1929951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475310
Supporting Variants
Samples
Known GenesCCDC81, ME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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