A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6876255



Internal ID9925426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:141107644..141107855hg38UCSC Ensembl
Outerchr8:142117743..142117954hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737760, esv2737759, esv2737756
Supporting Variants
SamplesSSM092
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)essv6876255
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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