A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430837



Internal ID22488707
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 StatusS
Merged Variantsnsv5912589
Supporting Variants
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430837
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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