A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043875



Internal ID19133094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918534..18939191hg38UCSC Ensembl
Innerchr11:18940081..18960738hg19UCSC Ensembl
Innerchr11:18896657..18917314hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820658
hg1920658
hg1820658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3510633, nssv3515687
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)nsv1043875
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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