A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6913598



Internal ID9677780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63723359..63723731hg38UCSC Ensembl
Outerchr20:62354711..62355083hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722961, esv2722959, esv2722960
Supporting Variants
SamplesSSM015
Known GenesZGPAT
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)essv6913598
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