A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6808967



Internal ID9863789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:142877664..142915660hg38UCSC Ensembl
Outerchr8:143959080..143997076hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3837997
hg1937997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737938
Supporting Variants
SamplesSSM075
Known GenesCYP11B1, CYP11B2
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)essv6808967
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