A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927686



Internal ID21347755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20338388..20338388hg38UCSC Ensembl
chr22:20325911..20325911hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382836
hg192836
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189145, nssv15189146
SamplesHG002
Known GenesLOC729444
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927686
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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