A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6696682



Internal ID10109940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15651107..15651573hg38UCSC Ensembl
Outerchr19:15761917..15762383hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718235, esv2718237
Supporting Variants
SamplesSSM037
Known GenesCYP4F3
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)essv6696682
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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