A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6948525



Internal ID9708948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143273633..143274080hg38UCSC Ensembl
Outerchr8:144355803..144356250hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737985, esv2737986, esv2737982
Supporting Variants
SamplesSSM024
Known GenesGLI4
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)essv6948525
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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