A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409953



Internal ID22467823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3288766..3324902hg38UCSC Ensembl
chr4:3290493..3326629hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3836137
hg1936137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894246
Supporting Variants
Samples
Known GenesRGS12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409953
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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