A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989276



Internal ID12974278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928910..18940132hg38UCSC Ensembl
Innerchr11:18950457..18961679hg19UCSC Ensembl
Innerchr11:18907033..18918255hg18UCSC Ensembl
Innerchr11:18907033..18918255hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811223
hg1911223
hg1811223
hg1711223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751005
Supporting Variants
SamplesBEC_512
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989276
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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