A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6768658



Internal ID9827359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98653880..98654058hg38UCSC Ensembl
Outerchr13:99306134..99306312hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747861, esv2747864, esv2747862
Supporting Variants
SamplesSSM064
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)essv6768658
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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