A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2731426



Internal ID10315062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:1441316..1441537hg38UCSC Ensembl
Outerchr6:1441551..1441772hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6837323, essv6822359, essv6764926, essv6782080, essv6798729, essv6719307, essv6694052, essv6690326, essv6930346, essv6711736, essv6893398, essv6814223, essv6818081, essv6670970, essv6963558, essv6956835
SamplesSSM036, SSM083, SSM027, SSM079, SSM042, SSM026, SSM031, SSM044, SSM068, SSM072, SSM020, SSM078, SSM037, SSM077, SSM098, SSM063
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)esv2731426
Frequency
Sample Size96
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer