A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5849702



Internal ID8950015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2730827..2731018hg38UCSC Ensembl
chr19:2730825..2731016hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677397
Supporting Variants
SamplesHG00500
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5849702
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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