A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021238



Internal ID18763772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..413750hg38UCSC Ensembl
Innerchr8:46386..363750hg19UCSC Ensembl
Innerchr8:36386..353750hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38317365
hg19317365
hg18317365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6789n100
Supporting Variantsnssv3674898
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)nsv1021238
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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