A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3398090



Internal ID14898367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1524253..1526051hg38UCSC Ensembl
Innerchr19:1525051..1525253hg38UCSC Ensembl
Outerchr19:1523253..1527051hg38UCSC Ensembl
chr19:1524252..1526050hg19UCSC Ensembl
Innerchr19:1525050..1525252hg19UCSC Ensembl
Outerchr19:1523252..1527050hg19UCSC Ensembl
chr19:1475252..1477050hg18UCSC Ensembl
Innerchr19:1476252..1476050hg18UCSC Ensembl
Outerchr19:1474252..1478050hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8691410
SamplesNA19239
Known GenesPLK5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3398090
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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