A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038189



Internal ID18780720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67577849..67981775hg38UCSC Ensembl
Innerchr11:67345320..67749246hg19UCSC Ensembl
Innerchr11:67101896..67505822hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38403927
hg19403927
hg18403927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1214n100
Supporting Variantsnssv3508313
Samples
Known GenesACY3, ALDH3B2, DOC2GP, FAM86C2P, GSTP1, NDUFV1, NUDT8, TBX10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038189
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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