A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694362



Internal ID21216214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126947647..126947647hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383719
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694362
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