A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1071n100



Internal ID22787158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18929947..18949854hg38UCSC Ensembl
chr11:18951494..18971401hg19UCSC Ensembl
chr11:18908070..18927977hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819908
hg1919908
hg1819908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044311, nsv1044861
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)dgv1071n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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