A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478833



Internal ID256379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9961023..9977706hg38UCSC Ensembl
chr8:9818533..9835216hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3816684
hg1916684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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