A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6691111



Internal ID9757520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:125669143..125669450hg38UCSC Ensembl
Outerchr8:126681387..126681694hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737553, esv2737545
Supporting Variants
SamplesSSM036
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)essv6691111
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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