A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588575



Internal ID21780618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21981206..21981264hg38UCSC Ensembl
chr9:21981205..21981263hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008460
Supporting Variants
Samples
Known GenesCDKN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588575
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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