A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505974



Internal ID282732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107682031..107787122hg38UCSC Ensembl
chr11:107552757..107657848hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38105092
hg19105092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050695
Samples
Known GenesSLN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505974
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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