A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2741652



Internal ID10295768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105666832..105767870hg38UCSC Ensembl
Outerchr14:106133169..106234207hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38101039
hg19101039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv287e201
Supporting Variantsessv6772417
SamplesSSM065
Known GenesELK2AP
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)esv2741652
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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