A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6926307



Internal ID9987574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:81389636..81390693hg38UCSC Ensembl
Outerchr5:80685455..80686512hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730381
Supporting Variants
SamplesSSM003
Known GenesACOT12, RNU5D-1, RNU5E-1
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)essv6926307
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