A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050222



Internal ID19139441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18937331hg38UCSC Ensembl
Innerchr11:18940322..18958878hg19UCSC Ensembl
Innerchr11:18896898..18915454hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3818557
hg1918557
hg1818557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3519519
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)nsv1050222
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