A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224952



Internal ID20791992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21005579..21160083hg38UCSC Ensembl
chr9:21005578..21160082hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38154505
hg19154505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432602
Supporting Variants
Samples
Known GenesIFNB1, IFNW1, PTPLAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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