A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521774



Internal ID18820055
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 StatusS
Merged Variantsnsv1051813
Supporting Variants
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)nssv3521774
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer