A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178474



Internal ID20745514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46939309..46941560hg38UCSC Ensembl
chr11:46960860..46963111hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456816
Supporting Variants
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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