A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161411



Internal ID8252672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96081345..96100001hg38UCSC Ensembl
Innerchr11:95814509..95833165hg19UCSC Ensembl
Innerchr11:95454157..95472813hg18UCSC Ensembl
Innerchr11:95454157..95472813hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3818657
hg1918657
hg1818657
hg1718657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2422272
Supporting Variants
SamplesND01496
Known GenesMAML2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161411
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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