A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067413



Internal ID19156632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73758387..73958167hg38UCSC Ensembl
Innerchr18:71425622..71625402hg19UCSC Ensembl
Innerchr18:69576602..69776382hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38199781
hg19199781
hg18199781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723229
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)nsv1067413
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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