A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047141



Internal ID19136360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929027..18940179hg38UCSC Ensembl
Innerchr11:18950574..18961726hg19UCSC Ensembl
Innerchr11:18907150..18918302hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811153
hg1911153
hg1811153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3522663, nssv3511627
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047141
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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