A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6764128



Internal ID9823651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42569812..42570602hg38UCSC Ensembl
Outerchr21:43989922..43990712hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723556
Supporting Variants
SamplesSSM062
Known GenesSLC37A1
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)essv6764128
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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