A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920364



Internal ID9683918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:45377873..45382072hg38UCSC Ensembl
Outerchr13:45952008..45956207hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747343, esv2747342, esv2747344
Supporting Variants
SamplesSSM017
Known GenesTPT1-AS1
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)essv6920364
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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