A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6668284



Internal ID9738579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:25370973..25371687hg38UCSC Ensembl
Outerchr13:25945111..25945825hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747161, esv2747168
Supporting Variants
SamplesSSM030
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)essv6668284
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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