A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1067n100



Internal ID22787154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18927513..18940804hg38UCSC Ensembl
chr11:18949060..18962351hg19UCSC Ensembl
chr11:18905636..18918927hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3813292
hg1913292
hg1813292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045979, nsv1040491, nsv1041452, nsv1053218, nsv1037747, nsv1051894, nsv1047141, nsv1048197, nsv1041835, nsv1046744, nsv1048018, nsv1052075, nsv1042305, nsv1054083, nsv1048562, nsv1048735, nsv1055003, nsv1046645, nsv1035672, nsv1052856, nsv1042356, nsv1054264, nsv1037057
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)dgv1067n100
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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