A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018514



Internal ID18761047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21944276..22075327hg38UCSC Ensembl
Innerchr9:21944275..22075326hg19UCSC Ensembl
Innerchr9:21934275..22065326hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38131052
hg19131052
hg18131052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690719
Samples
Known GenesC9orf53, CDKN2A, CDKN2B, CDKN2B-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018514
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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