A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1130803



Internal ID15637303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22006270..22009961hg38UCSC Ensembl
Innerchr9:22006269..22009960hg19UCSC Ensembl
Innerchr9:21996269..21999960hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383692
hg193692
hg183692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613760
Supporting Variants
Samples
Known GenesCDKN2B, CDKN2B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1130803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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