A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919252



Internal ID22694474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92682783..92684860hg38UCSC Ensembl
chr11:92415949..92418026hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369445
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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