A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032564



Internal ID18775098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..448710hg38UCSC Ensembl
Innerchr8:46386..398710hg19UCSC Ensembl
Innerchr8:36386..388710hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38352325
hg19352325
hg18352325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6789n100
Supporting Variantsnssv3674901, nssv3674899, nssv3674900
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032564
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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