A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6666418



Internal ID9733239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19885376..19885597hg38UCSC Ensembl
Outerchr19:19996185..19996406hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718299, esv2718298, esv2718296, esv2718297
Supporting Variants
SamplesSSM029
Known GenesZNF253
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)essv6666418
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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