A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046524



Internal ID19135743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256759..80271129hg38UCSC Ensembl
Innerchr11:79967803..79982173hg19UCSC Ensembl
Innerchr11:79645451..79659821hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814371
hg1914371
hg1814371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1236n100
Supporting Variantsnssv3513047
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)nsv1046524
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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