A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161366



Internal ID8252832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:5628081..6267407hg38UCSC Ensembl
Innerchr8:5485603..6124928hg19UCSC Ensembl
Innerchr8:5473011..6112336hg18UCSC Ensembl
Innerchr8:5473011..6112336hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38639327
hg19639326
hg18639326
hg17639326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422369
Supporting Variants
SamplesND03713
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161366
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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