A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682454



Internal ID21204312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35153671..35153671hg38UCSC Ensembl
chr20:33741474..33741474hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682454
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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