A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930918



Internal ID21350988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30454536..30454536hg38UCSC Ensembl
chr22:30850523..30850523hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189952
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930918
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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