A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686360



Internal ID21208217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31510484..31510537hg38UCSC Ensembl
chr15:31802687..31802740hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795052
Supporting Variants
Samples
Known GenesOTUD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686360
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03125


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