A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107411



Internal ID2623171
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644920
Supporting Variants
SamplesHG02318
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107411
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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