A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6912891



Internal ID9674861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:65611025..65611445hg38UCSC Ensembl
Outerchr14:66077743..66078163hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748797, esv2748798, esv2748779
Supporting Variants
SamplesSSM015
Known GenesFUT8
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)essv6912891
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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