A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789866



Internal ID21235204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117320378..117320535hg38UCSC Ensembl
chr11:117191094..117191251hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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