A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146724



Internal ID345929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41967100..41973564hg38UCSC Ensembl
chr22:42363104..42369568hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg386465
hg196465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146724
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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