A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015475



Internal ID18758009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43284180..43726076hg38UCSC Ensembl
Innerchr8:43139323..43581219hg19UCSC Ensembl
Innerchr8:43258480..43700376hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38441897
hg19441897
hg18441897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7188n100
Supporting Variantsnssv3687273
Samples
Known GenesPOTEA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015475
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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