A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643420



Internal ID6683495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2296779..2301990hg38UCSC Ensembl
Innerchr19:2297279..2301490hg38UCSC Ensembl
Outerchr19:2295779..2302990hg38UCSC Ensembl
chr19:2296778..2301989hg19UCSC Ensembl
Innerchr19:2297278..2301489hg19UCSC Ensembl
Outerchr19:2295778..2302989hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385212
hg195212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15969538
SamplesNA18959
Known GenesLINGO3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643420
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer