A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6842131



Internal ID9661210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:53185938..53188748hg38UCSC Ensembl
Outerchr19:53689191..53692001hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718787, esv2718812, esv2718813
Supporting Variants
SamplesSSM010
Known GenesZNF665
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)essv6842131
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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