A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491655



Internal ID268887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96533561..96533710hg38UCSC Ensembl
chr8:97545789..97545938hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016123
Samples
Known GenesSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491655
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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