A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050041



Internal ID101257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95187998..95189421hg38UCSC Ensembl
chr11:94921162..94922585hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499318
Supporting Variants
Samples
Known GenesSESN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050041
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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