A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492023



Internal ID269248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93468222..93486222hg38UCSC Ensembl
chr8:94480450..94498450hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013556
Samples
Known GenesLINC00535
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492023
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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