A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6855026



Internal ID9906321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:168665631..168665711hg38UCSC Ensembl
Outerchr5:168092636..168092716hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731044, esv2731045
Supporting Variants
SamplesSSM087
Known GenesSLIT3
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)essv6855026
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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