A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554016



Internal ID16341425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37739134..37848142hg38UCSC Ensembl
Innerchr11:37760684..37869692hg19UCSC Ensembl
Innerchr11:37717260..37826268hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38109009
hg19109009
hg18109009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1746n54
Supporting Variantsnssv771073
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554016
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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