A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644920



Internal ID7031671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58012890..58016965hg38UCSC Ensembl
Innerchr19:58012909..58016947hg38UCSC Ensembl
Outerchr19:58012872..58016984hg38UCSC Ensembl
chr19:58524258..58528333hg19UCSC Ensembl
Innerchr19:58524277..58528315hg19UCSC Ensembl
Outerchr19:58524240..58528352hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384076
hg194076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107410, essv16107411
SamplesHG01402, HG02318
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644920
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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