A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553794



Internal ID15994517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24413656..24516078hg38UCSC Ensembl
Innerchr11:24435202..24537624hg19UCSC Ensembl
Innerchr11:24391778..24494200hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38102423
hg19102423
hg18102423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1702n54
Supporting Variantsnssv768989
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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