A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029889



Internal ID19119108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22118047..22161829hg38UCSC Ensembl
Innerchr9:22118046..22161828hg19UCSC Ensembl
Innerchr9:22108046..22151828hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3843783
hg1943783
hg1843783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690720
Samples
Known GenesCDKN2B-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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