A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1682n54



Internal ID22769577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18928069..18943568hg38UCSC Ensembl
chr11:18949616..18965115hg19UCSC Ensembl
chr11:18906192..18921691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815500
hg1915500
hg1815500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553662, nsv553659, nsv553661, nsv553663, nsv553665
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1682n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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