A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6694899



Internal ID10107193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:98067680..98069365hg38UCSC Ensembl
Outerchr8:99079908..99081593hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg381686
hg191686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737347
Supporting Variants
SamplesSSM037
Known GenesC8orf47
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6694899
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer