A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236932



Internal ID20803972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22090101..22096100hg38UCSC Ensembl
chr9:22090100..22096099hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425872
Supporting Variants
Samples
Known GenesCDKN2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00126


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