A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911029



Internal ID22686241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84769821..84769940hg38UCSC Ensembl
chr11:84480864..84480983hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357624
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911029
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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