A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987616



Internal ID12977159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18940132hg38UCSC Ensembl
Innerchr11:18940322..18961679hg19UCSC Ensembl
Innerchr11:18896898..18918255hg18UCSC Ensembl
Innerchr11:18896898..18918255hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821358
hg1921358
hg1821358
hg1721358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750995
Supporting Variants
SamplesBEC_717
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987616
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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