A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6949082



Internal ID10055133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:11168252..11168394hg38UCSC Ensembl
Outerchr12:11320851..11320993hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745553, esv2745554
Supporting Variants
SamplesSSM024
Known GenesPRH1-PRR4
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)essv6949082
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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