A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985196



Internal ID12636271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18927673..18935650hg38UCSC Ensembl
Innerchr11:18949220..18957197hg19UCSC Ensembl
Innerchr11:18905796..18913773hg18UCSC Ensembl
Innerchr11:18905796..18913773hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387978
hg197978
hg187978
hg177978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750987
Supporting Variants
SamplesSPC_124
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985196
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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