A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707205



Internal ID21229003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3504672..3504672hg38UCSC Ensembl
chr9:3504672..3504672hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818791
Supporting Variants
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707205
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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