A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2718058



Internal ID9952349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6024798..6024899hg38UCSC Ensembl
Outerchr19:6024809..6024910hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6858696, essv6863557
SamplesSSM088, SSM087
Known GenesRFX2
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)esv2718058
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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