A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018959



Internal ID19108176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11537723..11598247hg38UCSC Ensembl
Innerchr8:11395232..11455756hg19UCSC Ensembl
Innerchr8:11432641..11493165hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3860525
hg1960525
hg1860525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7014n100
Supporting Variantsnssv3681735
Samples
Known GenesBLK, LINC00208
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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