A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479965



Internal ID257478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35610514..35616819hg38UCSC Ensembl
chr8:35468032..35474337hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386306
hg196306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010485
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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