A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925650



Internal ID21345723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35631629..35631629hg38UCSC Ensembl
chr22:36027676..36027676hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187409
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925650
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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