A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926908



Internal ID21346979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884128..10884128hg38UCSC Ensembl
chr16:10977985..10977985hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195536
SamplesHG002
Known GenesCIITA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926908
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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