A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983854



Internal ID12976059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18882057..18940132hg38UCSC Ensembl
Innerchr11:18903604..18961679hg19UCSC Ensembl
Innerchr11:18860180..18918255hg18UCSC Ensembl
Innerchr11:18860180..18918255hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3858076
hg1958076
hg1858076
hg1758076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750988
Supporting Variants
SamplesBEC_635
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983854
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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