A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289349



Internal ID20498567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21980974..21981109hg38UCSC Ensembl
chr9:21980973..21981108hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744198
Supporting Variants
Samples
Known GenesCDKN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289349
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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