A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1061n100



Internal ID22787148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18911502..18940804hg38UCSC Ensembl
chr11:18933049..18962351hg19UCSC Ensembl
chr11:18889625..18918927hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3829303
hg1929303
hg1829303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036746, nsv1050116, nsv1053235, nsv1051310, nsv1042291, nsv1048260, nsv1043706, nsv1038590, nsv1039556, nsv1051813
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)dgv1061n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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