A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555072



Internal ID21879427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184430311..184430311hg38UCSC Ensembl
chr4:185351465..185351465hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076425
Supporting Variants
Samples
Known GenesIRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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