A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553791



Internal ID15994514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24385835..24506412hg38UCSC Ensembl
Innerchr11:24407381..24527958hg19UCSC Ensembl
Innerchr11:24363957..24484534hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38120578
hg19120578
hg18120578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1702n54
Supporting Variantsnssv1174758
SamplesNINDS_94
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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