A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022313



Internal ID18764847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27083371..27250507hg38UCSC Ensembl
Innerchr9:27083369..27250505hg19UCSC Ensembl
Innerchr9:27073369..27240505hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38167137
hg19167137
hg18167137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7487n100
Supporting Variantsnssv3692008
Samples
Known GenesLINC00032, TEK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022313
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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