A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466522



Internal ID244356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108757226..108762007hg38UCSC Ensembl
chr6:109078429..109083210hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384782
hg194782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986745
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466522
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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