A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043503



Internal ID19132722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55172866hg38UCSC Ensembl
Innerchr11:54720811..54940342hg19UCSC Ensembl
Innerchr11:54477387..54696918hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38219532
hg19219532
hg18219532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1160n100
Supporting Variantsnssv3510021
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)nsv1043503
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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