A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553663



Internal ID16341072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929590..18943568hg38UCSC Ensembl
Innerchr11:18951137..18965115hg19UCSC Ensembl
Innerchr11:18907713..18921691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3813979
hg1913979
hg1813979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1682n54
Supporting Variantsnssv768668, nssv768667
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553663
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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