A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981345



Internal ID12973208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18953905hg38UCSC Ensembl
Innerchr11:18940322..18975452hg19UCSC Ensembl
Innerchr11:18896898..18932028hg18UCSC Ensembl
Innerchr11:18896898..18932028hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3835131
hg1935131
hg1835131
hg1735131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750997
Supporting Variants
SamplesBEC_389
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981345
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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