A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399211



Internal ID14899488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35296409..35299107hg38UCSC Ensembl
Innerchr19:35297409..35298107hg38UCSC Ensembl
Outerchr19:35295409..35300107hg38UCSC Ensembl
chr19:35787312..35790010hg19UCSC Ensembl
Innerchr19:35788312..35789010hg19UCSC Ensembl
Outerchr19:35786312..35791010hg19UCSC Ensembl
chr19:40479152..40481850hg18UCSC Ensembl
Innerchr19:40480152..40480850hg18UCSC Ensembl
Outerchr19:40478152..40482850hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2010e59
Supporting Variantsessv8691521
SamplesNA19240
Known GenesMAG
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399211
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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