A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491895



Internal ID269122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35698166..35698239hg38UCSC Ensembl
chr8:35555684..35555757hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010488
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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