A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047460



Internal ID18789991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89512864..89727875hg38UCSC Ensembl
Innerchr9:92127779..92342790hg19UCSC Ensembl
Innerchr9:91317599..91532610hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38215012
hg19215012
hg18215012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697543
Samples
Known GenesGADD45G, UNQ6494
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047460
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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