A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146311



Internal ID345516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28661564..28667564hg38UCSC Ensembl
chr22:29057552..29063552hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728309
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146311
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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