A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985602



Internal ID12972300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928910..18962848hg38UCSC Ensembl
Innerchr11:18950457..18984395hg19UCSC Ensembl
Innerchr11:18907033..18940971hg18UCSC Ensembl
Innerchr11:18907033..18940971hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3833939
hg1933939
hg1833939
hg1733939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751020
Supporting Variants
SamplesBEC_299
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985602
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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