A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009166



Internal ID18751697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65104345..65215491hg38UCSC Ensembl
Innerchr1:65570028..65681174hg19UCSC Ensembl
Innerchr1:65342616..65453762hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38111147
hg19111147
hg18111147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv173n100
Supporting Variantsnssv3482627
Samples
Known GenesAK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009166
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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