A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6964868



Internal ID10072177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:140195571..140195870hg38UCSC Ensembl
Outerchr8:141205670..141205969hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737750, esv2737749
Supporting Variants
SamplesSSM027
Known GenesTRAPPC9
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)essv6964868
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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