A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049986



Internal ID101220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94374439..94390344hg38UCSC Ensembl
chr11:94107605..94123510hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3815906
hg1915906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501054
Supporting Variants
Samples
Known GenesGPR83
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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