A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2723679



Internal ID9957979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44733362..44733480hg38UCSC Ensembl
Outerchr21:46153277..46153395hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6859100, essv6909981, essv6675127, essv6863865
SamplesSSM087, SSM088, SSM031, SSM014
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)esv2723679
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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