A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985511



Internal ID20552551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102903228..102916957hg38UCSC Ensembl
chr11:102773958..102787687hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3813730
hg1913730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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