A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050863



Internal ID101791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90144423..90144516hg38UCSC Ensembl
chr11:89877591..89877684hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502902
Supporting Variants
Samples
Known GenesNAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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