A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6818404



Internal ID10220800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165708813..165708968hg38UCSC Ensembl
Outerchr6:166122301..166122456hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733153, esv2733152
Supporting Variants
SamplesSSM078
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)essv6818404
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