A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911009



Internal ID22686221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33560668..33562655hg38UCSC Ensembl
chr8:33418186..33420173hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381988
hg191988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441610
Samples
Known GenesRNF122
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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