A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669225



Internal ID21617530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41610080..41610080hg38UCSC Ensembl
chr22:42006084..42006084hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134012
SamplesNA20847
Known GenesDESI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669225
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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