A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043979



Internal ID19133198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918534..18940574hg38UCSC Ensembl
Innerchr11:18940081..18962121hg19UCSC Ensembl
Innerchr11:18896657..18918697hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822041
hg1922041
hg1822041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3507535
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)nsv1043979
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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