A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2717834



Internal ID5065124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1208925..1209218hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6797062, essv6678825, essv6674726, essv6703479
SamplesSSM031, SSM071, SSM032, SSM039
Known GenesSTK11
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2717834
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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