A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6905997



Internal ID10016477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10009886..10010320hg38UCSC Ensembl
Outerchr21:10487914..10488348hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723063, esv2723060
Supporting Variants
SamplesSSM013
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)essv6905997
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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