A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6828875



Internal ID10229470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10798762..10799337hg38UCSC Ensembl
Outerchr21:10713120..10713695hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723085, esv2723077, esv2723087, esv2723079, esv2723082, esv2723086
Supporting Variants
SamplesSSM080
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)essv6828875
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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