A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488546



Internal ID265854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78691640..78697506hg38UCSC Ensembl
chr10:80451397..80457263hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385867
hg195867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488546
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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