A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476065



Internal ID253686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77473114..77473428hg38UCSC Ensembl
chr8:78385350..78385664hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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