A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689275



Internal ID21211128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28224007..28224007hg38UCSC Ensembl
chr17:26551033..26551033hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689275
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.346154


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