A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422272



Internal ID8253055
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161411
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)esv2422272
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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