A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912589



Internal ID22687805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27194806..27296013hg38UCSC Ensembl
chr9:27194804..27296011hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38101208
hg19101208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430837
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912589
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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