A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187409



Internal ID21326242
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925650
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187409
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