A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2745887



Internal ID10326857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:51718175..51719701hg38UCSC Ensembl
Outerchr12:52111959..52113485hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6977224
SamplesSSM029
Known GenesSCN8A
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)esv2745887
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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