A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6936455



Internal ID9698878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:70424307..70425443hg38UCSC Ensembl
Outerchr14:70891024..70892160hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748837
Supporting Variants
SamplesSSM021
Known Genes
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)essv6936455
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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