A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697083



Internal ID21218932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106285865..106285865hg38UCSC Ensembl
chr8:107298093..107298093hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816861
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697083
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.265625


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