A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6874493



Internal ID9923839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:53736177..53745504hg38UCSC Ensembl
Outerchr19:54239431..54248758hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg389328
hg199328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718833, esv2718812, esv2718838
Supporting Variants
SamplesSSM091
Known GenesMIR516B1, MIR517C, MIR518A2, MIR520H
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)essv6874493
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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