A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv41e55



Internal ID22760991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18891674..18961087hg38UCSC Ensembl
chr11:18913221..18982634hg19UCSC Ensembl
chr11:18869797..18939210hg18UCSC Ensembl
chr11:18869797..18939210hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3869414
hg1969414
hg1869414
hg1769414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2750991, esv2750989
SamplesBEC_543, BEC_576
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv41e55
Frequency
Sample Size771
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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