A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033031



Internal ID18775565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9452756..9561431hg38UCSC Ensembl
Innerchr8:9310266..9418941hg19UCSC Ensembl
Innerchr8:9347676..9456351hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38108676
hg19108676
hg18108676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681708
Samples
Known GenesTNKS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033031
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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