A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489178



Internal ID266466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78443105..78443192hg38UCSC Ensembl
chr10:80202862..80202949hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489178
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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