A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408119



Internal ID187449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26641271..26641322hg38UCSC Ensembl
chr6:26641499..26641550hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982394
Samples
Known GenesZNF322
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408119
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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