A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6963081



Internal ID10068858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:174265133..174265527hg38UCSC Ensembl
Outerchr4:175186284..175186678hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2728766
Supporting Variants
SamplesSSM027
Known GenesFBXO8
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)essv6963081
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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