A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798646



Internal ID21243984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10377666..10377666hg38UCSC Ensembl
chr19:10488342..10488342hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682084
Samples
Known GenesTYK2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798646
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