A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934399



Internal ID21354468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32331001..32331001hg38UCSC Ensembl
chr22:32726988..32726988hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189960
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934399
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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