A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981346



Internal ID12973209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18927673..18949439hg38UCSC Ensembl
Innerchr11:18949220..18970986hg19UCSC Ensembl
Innerchr11:18905796..18927562hg18UCSC Ensembl
Innerchr11:18905796..18927562hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821767
hg1921767
hg1821767
hg1721767
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981346
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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