A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6773382



Internal ID10177860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45859132..45859526hg38UCSC Ensembl
Outerchr21:47279046..47279440hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723813
Supporting Variants
SamplesSSM065
Known GenesPCBP3
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)essv6773382
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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