A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178361



Internal ID20745401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17240542..17270435hg38UCSC Ensembl
chr11:17262089..17291982hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3829894
hg1929894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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