A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504529



Internal ID281329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105887225..105939749hg38UCSC Ensembl
chr11:105757951..105810475hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3852525
hg1952525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049073
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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