A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6851291



Internal ID10249643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:105378684..105378743hg38UCSC Ensembl
Outerchr12:105772462..105772521hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746325, esv2746324
Supporting Variants
SamplesSSM086
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)essv6851291
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