A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994051



Internal ID20561091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83302119..83302733hg38UCSC Ensembl
chr11:83013162..83013776hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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