A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1064n100



Internal ID22787151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18918534..18940574hg38UCSC Ensembl
chr11:18940081..18962121hg19UCSC Ensembl
chr11:18896657..18918697hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822041
hg1922041
hg1822041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047393, nsv1051288, nsv1040695, nsv1048566, nsv1044319, nsv1041267, nsv1046266, nsv1045442
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)dgv1064n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer