A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643669



Internal ID6683740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11307253..11311459hg38UCSC Ensembl
Innerchr19:11307271..11311442hg38UCSC Ensembl
Outerchr19:11307236..11311477hg38UCSC Ensembl
chr19:11417929..11422135hg19UCSC Ensembl
Innerchr19:11417947..11422118hg19UCSC Ensembl
Outerchr19:11417912..11422153hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384207
hg194207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990783
SamplesNA11831
Known GenesTSPAN16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643669
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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