A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017865



Internal ID18760398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11520286..11722445hg38UCSC Ensembl
Innerchr8:11377795..11579954hg19UCSC Ensembl
Innerchr8:11415204..11617363hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38202160
hg19202160
hg18202160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3754239
Samples
Known GenesBLK, GATA4, LINC00208
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017865
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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