A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643802



Internal ID7030559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16700529..16703597hg38UCSC Ensembl
Innerchr19:16700563..16703564hg38UCSC Ensembl
Outerchr19:16700496..16703631hg38UCSC Ensembl
chr19:16811340..16814408hg19UCSC Ensembl
Innerchr19:16811374..16814375hg19UCSC Ensembl
Outerchr19:16811307..16814442hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383069
hg193069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002825
SamplesHG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643802
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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