A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6925099



Internal ID10032012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:12231060..12231479hg38UCSC Ensembl
Outerchr18:12231059..12231478hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716811
Supporting Variants
SamplesSSM018
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)essv6925099
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