A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051813



Internal ID19141032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18912353..18940804hg38UCSC Ensembl
Innerchr11:18933900..18962351hg19UCSC Ensembl
Innerchr11:18890476..18918927hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3828452
hg1928452
hg1828452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1061n100
Supporting Variantsnssv3521774
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)nsv1051813
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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