A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553661



Internal ID16341070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929590..18940934hg38UCSC Ensembl
Innerchr11:18951137..18962481hg19UCSC Ensembl
Innerchr11:18907713..18919057hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811345
hg1911345
hg1811345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1682n54
Supporting Variantsnssv768664
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553661
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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