A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6775722



Internal ID10181631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:55608504..55610442hg38UCSC Ensembl
Outerchr12:56002288..56004226hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg381939
hg191939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745924
Supporting Variants
SamplesSSM066
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)essv6775722
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