A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045481



Internal ID19134700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133589978..133693596hg38UCSC Ensembl
Innerchr11:133459873..133563491hg19UCSC Ensembl
Innerchr11:132965083..133068701hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38103619
hg19103619
hg18103619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514154
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)nsv1045481
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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