A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6873649



Internal ID9923081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:8864315..8865444hg38UCSC Ensembl
Outerchr12:9016911..9018040hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381130
hg191130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745509
Supporting Variants
SamplesSSM091
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)essv6873649
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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