A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6821486



Internal ID9876134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:54338356..54340368hg38UCSC Ensembl
Outerchr2:54565493..54567505hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720078, esv2720080
Supporting Variants
SamplesSSM079
Known GenesC2orf73
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)essv6821486
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