A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643819



Internal ID7030576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17465840..17470094hg38UCSC Ensembl
Innerchr19:17465862..17470072hg38UCSC Ensembl
Outerchr19:17465818..17470116hg38UCSC Ensembl
chr19:17576649..17580903hg19UCSC Ensembl
Innerchr19:17576671..17580881hg19UCSC Ensembl
Outerchr19:17576627..17580925hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384255
hg194255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16003677, essv16003678
SamplesHG03600, HG02465
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643819
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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