A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016733



Internal ID18759268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27073652..27264578hg38UCSC Ensembl
Innerchr9:27073650..27264576hg19UCSC Ensembl
Innerchr9:27063650..27254576hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38190927
hg19190927
hg18190927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7487n100
Supporting Variantsnssv3692007
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)nsv1016733
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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