A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3273496



Internal ID11293162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:11388052..11389701hg38UCSC Ensembl
Outerchr8:11245561..11247210hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7543063
SamplesHuRef
Known GenesC8orf12
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3273496
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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