A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6823955



Internal ID10225041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:103131830..103132192hg38UCSC Ensembl
Outerchr14:103598167..103598529hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749162
Supporting Variants
SamplesSSM079
Known GenesTNFAIP2
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)essv6823955
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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