A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796035



Internal ID21241373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55687191..55687191hg38UCSC Ensembl
chr16:55721103..55721103hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704183
Samples
Known GenesSLC6A2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796035
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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