A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5945488



Internal ID8922891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6533305..6535411hg38UCSC Ensembl
Outerchr19:6532734..6535881hg38UCSC Ensembl
Innerchr19:6533316..6535422hg19UCSC Ensembl
Outerchr19:6532745..6535892hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668569
Supporting Variants
SamplesNA19700
Known GenesTNFSF9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5945488
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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