A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923733



Internal ID22698960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8422993..8425057hg38UCSC Ensembl
chr11:8444540..8446604hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368746
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923733
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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