A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789740



Internal ID21235078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121329247..121329247hg38UCSC Ensembl
chr11:121199956..121199956hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789740
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