A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020182



Internal ID18762718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:162784..453258hg38UCSC Ensembl
Innerchr8:112784..403258hg19UCSC Ensembl
Innerchr8:102784..393258hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38290475
hg19290475
hg18290475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6791n100
Supporting Variantsnssv3674915
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)nsv1020182
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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