A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023856



Internal ID19113073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:162784..244891hg38UCSC Ensembl
Innerchr8:112784..194891hg19UCSC Ensembl
Innerchr8:102784..184891hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3882108
hg1982108
hg1882108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6790n100
Supporting Variantsnssv3674909, nssv3674910
Samples
Known GenesOR4F21, 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)nsv1023856
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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