A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6863600



Internal ID9910264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:22958004..22960098hg38UCSC Ensembl
Outerchr19:23140806..23142900hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382095
hg192095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718337, esv2718366
Supporting Variants
SamplesSSM088
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)essv6863600
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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