A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048659



Internal ID100313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78978131..78978206hg38UCSC Ensembl
chr11:78689176..78689251hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512900
Supporting Variants
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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