A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789752



Internal ID21235090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124296755..124296755hg38UCSC Ensembl
chr11:124166651..124166651hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789752
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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