A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053811



Internal ID18796342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67581973..67981775hg38UCSC Ensembl
Innerchr11:67349444..67749246hg19UCSC Ensembl
Innerchr11:67106020..67505822hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38399803
hg19399803
hg18399803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1214n100
Supporting Variantsnssv3710615, nssv3710614
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)nsv1053811
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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