A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6734248



Internal ID10143916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166867034..166867368hg38UCSC Ensembl
Outerchr5:166294039..166294373hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731032
Supporting Variants
SamplesSSM049
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)essv6734248
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