A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190916



Internal ID20757956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11944401..11968100hg38UCSC Ensembl
chr11:11965948..11989647hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3823700
hg1923700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448150
Supporting Variants
Samples
Known GenesDKK3, USP47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00089


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