A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985575



Internal ID12625439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107935064..108020064hg38UCSC Ensembl
Innerchr11:107805790..107890790hg19UCSC Ensembl
Innerchr11:107311000..107396000hg18UCSC Ensembl
Innerchr11:107311000..107396000hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3885001
hg1985001
hg1885001
hg1785001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750980
Supporting Variants
SamplesBEC_229
Known GenesCUL5, RAB39A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985575
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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