A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6733565



Internal ID9998368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:35089538..35090120hg38UCSC Ensembl
Outerchr8:34947056..34947638hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736872
Supporting Variants
SamplesSSM007
Known Genes
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)essv6733565
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