A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018236



Internal ID18760769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10057918..10082971hg38UCSC Ensembl
Innerchr8:9915428..9940481hg19UCSC Ensembl
Innerchr8:9952838..9977891hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3825054
hg1925054
hg1825054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681712
Samples
Known GenesMSRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018236
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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