A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2723038



Internal ID10306674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9040408..9042085hg38UCSC Ensembl
Outerchr21:9879241..9880918hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg381678
hg191678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6794042, essv6972131, essv6718034, essv6954551
SamplesSSM028, SSM001, SSM025, SSM043
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)esv2723038
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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