A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789869



Internal ID21235207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854060..11855019hg38UCSC Ensembl
chr11:11875607..11876566hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693010
Samples
Known GenesUSP47
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789869
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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