A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189916



Internal ID20756956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17298724..17302797hg38UCSC Ensembl
chr11:17320271..17324344hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454727
Supporting Variants
Samples
Known GenesNUCB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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