A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230651



Internal ID20797691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21937413..22077537hg38UCSC Ensembl
chr9:21937412..22077536hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38140125
hg19140125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418132
Supporting Variants
Samples
Known GenesC9orf53, CDKN2A, CDKN2B, CDKN2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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