A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231392



Internal ID20798432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27194806..27296014hg38UCSC Ensembl
chr9:27194804..27296012hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38101209
hg19101209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424722
Supporting Variants
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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