A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189514



Internal ID20756554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21535374..21718724hg38UCSC Ensembl
chr11:21556920..21740270hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38183351
hg19183351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440424
Supporting Variants
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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