A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161290



Internal ID7906004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35928148..36967365hg38UCSC Ensembl
Innerchr11:35949698..36988915hg19UCSC Ensembl
Innerchr11:35906274..36945491hg18UCSC Ensembl
Innerchr11:35906274..36945491hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381039218
hg191039218
hg181039218
hg171039218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422305
Supporting Variants
SamplesND04019
Known GenesC11orf74, COMMD9, LDLRAD3, MIR3973, PRR5L, RAG1, RAG2, TRAF6
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161290
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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