A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684248



Internal ID21206105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41293511..41293578hg38UCSC Ensembl
chr15:41585709..41585776hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795238
Supporting Variants
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684248
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.265625


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