A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6815449



Internal ID9870699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:11019977..11075680hg38UCSC Ensembl
Outerchr12:11172576..11228279hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855704
hg1955704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745546
Supporting Variants
SamplesSSM077
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)essv6815449
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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