A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018786



Internal ID19108003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85828719..85908817hg38UCSC Ensembl
Innerchr8:86840948..86921046hg19UCSC Ensembl
Innerchr8:86910236..86990162hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3880099
hg1980099
hg1879927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7260n100
Supporting Variantsnssv3757312
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018786
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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