A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553063



Internal ID15993786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1937879..1949501hg38UCSC Ensembl
Innerchr11:1959109..1970731hg19UCSC Ensembl
Innerchr11:1915685..1927307hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3811623
hg1911623
hg1811623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764478
Samples
Known GenesMRPL23, TNNT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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