A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687626



Internal ID21209480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599766..78599766hg38UCSC Ensembl
chr15:78892108..78892108hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795292
Supporting Variants
Samples
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687626
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