A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6909825



Internal ID9671010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52681666..52776111hg38UCSC Ensembl
Outerchr19:53184919..53279364hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3894446
hg1994446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718787, esv2718794, esv2718786
Supporting Variants
SamplesSSM014
Known GenesZNF600, ZNF611, ZNF83
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)essv6909825
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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