A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541837



Internal ID21866192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174434722..174434722hg38UCSC Ensembl
chr4:175355873..175355873hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541837
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