A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643539



Internal ID7030298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5793959..5797060hg38UCSC Ensembl
Innerchr19:5793959..5797060hg38UCSC Ensembl
Outerchr19:5793736..5797298hg38UCSC Ensembl
chr19:5793970..5797071hg19UCSC Ensembl
Innerchr19:5793970..5797071hg19UCSC Ensembl
Outerchr19:5793747..5797309hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15984167
SamplesNA18622
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643539
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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