A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553553



Internal ID15994276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13277469..13278005hg38UCSC Ensembl
Innerchr11:13299016..13299552hg19UCSC Ensembl
Innerchr11:13255592..13256128hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38537
hg19537
hg18537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1659n54
Supporting Variantsnssv768261
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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