A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2718689



Internal ID9952981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:48757636..48757786hg38UCSC Ensembl
Outerchr19:49260893..49261043hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6824686, essv6689083
SamplesSSM035, SSM079
Known GenesFGF21
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)esv2718689
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer