A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051894



Internal ID19141113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928314..18939843hg38UCSC Ensembl
Innerchr11:18949861..18961390hg19UCSC Ensembl
Innerchr11:18906437..18917966hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811530
hg1911530
hg1811530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3503134, nssv3522431
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)nsv1051894
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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