A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6969062



Internal ID9729325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1276636..1276786hg38UCSC Ensembl
Outerchr5:1276751..1276901hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729465, esv2729470, esv2729469
Supporting Variants
SamplesSSM028
Known GenesTERT
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)essv6969062
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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