A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909084



Internal ID22684294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63607915..63614743hg38UCSC Ensembl
chr11:63375387..63382215hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386829
hg196829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359497
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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