A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6977299



Internal ID10080901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:103982926..103984753hg38UCSC Ensembl
Outerchr12:104376704..104378531hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746304
Supporting Variants
SamplesSSM029
Known GenesTDG
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)essv6977299
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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