A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552858



Internal ID15993581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:557342..656845hg38UCSC Ensembl
Innerchr11:557342..656845hg19UCSC Ensembl
Innerchr11:547342..646845hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899504
hg1999504
hg1899504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1522n54
Supporting Variantsnssv1174587
SamplesHGDP00445
Known GenesC11orf35, CDHR5, DEAF1, DRD4, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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