A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553666



Internal ID16341075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18930975..18937264hg38UCSC Ensembl
Innerchr11:18952522..18958811hg19UCSC Ensembl
Innerchr11:18909098..18915387hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386290
hg196290
hg186290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768672
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553666
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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