A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794981



Internal ID21240319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65965604..65965604hg38UCSC Ensembl
chr15:66257942..66257942hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687538
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794981
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