A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161563



Internal ID8252878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59604198..59817739hg38UCSC Ensembl
Innerchr16:59638102..59851643hg19UCSC Ensembl
Innerchr16:58195603..58409144hg18UCSC Ensembl
Innerchr16:58195603..58409144hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38213542
hg19213542
hg18213542
hg17213542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422221
Supporting Variants
SamplesND04274
Known GenesAPOOP5
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161563
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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