A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688200



Internal ID21210055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40808121..40808121hg38UCSC Ensembl
chr15:41100319..41100319hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795235
Supporting Variants
Samples
Known GenesZFYVE19
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688200
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.16129


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