A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15999980



Internal ID5341378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15567761..15586004hg38UCSC Ensembl
Innerchr19:15567761..15586004hg38UCSC Ensembl
Outerchr19:15567261..15586504hg38UCSC Ensembl
chr19:15678572..15696815hg19UCSC Ensembl
Innerchr19:15678572..15696815hg19UCSC Ensembl
Outerchr19:15678072..15697315hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3818244
hg1918244
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643771
Supporting Variants
SamplesNA18877
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15999980
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