A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034121



Internal ID18776655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42694667..42763570hg38UCSC Ensembl
Innerchr8:42549810..42618713hg19UCSC Ensembl
Innerchr8:42668967..42737870hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3868904
hg1968904
hg1868904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7186n100
Supporting Variantsnssv3687266
Samples
Known GenesCHRNA6, CHRNB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034121
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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