A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948422



Internal ID21368491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37491606..37491606hg38UCSC Ensembl
chr22:37887644..37887644hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188790
SamplesHG002
Known GenesCARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948422
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer