A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542407



Internal ID21866762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1279040..1279040hg38UCSC Ensembl
chr4:1272828..1272828hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542407
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