A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6912572



Internal ID9675148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:11014851..11069989hg38UCSC Ensembl
Outerchr12:11167450..11222588hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855139
hg1955139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745546
Supporting Variants
SamplesSSM015
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
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)essv6912572
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