A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053918



Internal ID19143137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97038416..97226033hg38UCSC Ensembl
Innerchr11:96909416..97097033hg19UCSC Ensembl
Innerchr11:96414626..96602243hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38187618
hg19187618
hg18187618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521102
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)nsv1053918
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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