A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6876637



Internal ID9925768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:8864311..8865444hg38UCSC Ensembl
Outerchr12:9016907..9018040hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745509
Supporting Variants
SamplesSSM092
Known GenesA2ML1
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)essv6876637
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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