A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040491



Internal ID19129710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928798..18940804hg38UCSC Ensembl
Innerchr11:18950345..18962351hg19UCSC Ensembl
Innerchr11:18906921..18918927hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812007
hg1912007
hg1812007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3507711
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)nsv1040491
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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