A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192611



Internal ID20759651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50804801..50821400hg38UCSC Ensembl
chr11:50763972..50780519hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3816600
hg1916548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00431


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