A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6667299



Internal ID9644905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:53554975..53555366hg38UCSC Ensembl
Outerchr19:54058229..54058620hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718812, esv2718828
Supporting Variants
SamplesSSM004
Known GenesZNF331
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)essv6667299
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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