A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498156



Internal ID275159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108801784..108834966hg38UCSC Ensembl
chr11:108672511..108705693hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3833183
hg1933183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049156
Samples
Known GenesDDX10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498156
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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