A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6908863



Internal ID9671875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:11353437..11353628hg38UCSC Ensembl
Outerchr12:11506371..11506562hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745560, esv2745558
Supporting Variants
SamplesSSM014
Known GenesPRB1
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)essv6908863
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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