A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049061



Internal ID100591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105653606..105665500hg38UCSC Ensembl
chr11:105524333..105536227hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3811895
hg1911895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503718
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049061
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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