A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051066



Internal ID19140285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23438213..23528749hg38UCSC Ensembl
Innerchr11:23459759..23550295hg19UCSC Ensembl
Innerchr11:23416335..23506871hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3890537
hg1990537
hg1890537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513527
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)nsv1051066
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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