A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6780366



Internal ID9839124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:23774471..23774902hg38UCSC Ensembl
Outerchr20:23755108..23755539hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722310, esv2722308, esv2722305, esv2722309, esv2722303
Supporting Variants
SamplesSSM067
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)essv6780366
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer