A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193282



Internal ID20760322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16501651..16683925hg38UCSC Ensembl
chr11:16523198..16705472hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38182275
hg19182275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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