A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485655



Internal ID263039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55791095..55795246hg38UCSC Ensembl
chr8:56703654..56707805hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg384152
hg194152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012393
Samples
Known GenesTGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485655
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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