A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789885



Internal ID21235223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124296845..124296898hg38UCSC Ensembl
chr11:124166741..124166794hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789885
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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