A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678825



Internal ID9944930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44727637..44731001hg38UCSC Ensembl
Outerchr19:44727480..44731149hg38UCSC Ensembl
Innerchr19:45230899..45234266hg19UCSC Ensembl
Outerchr19:45230742..45234419hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383670
hg193678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647e199
Supporting Variantsessv5904928
SamplesHG00418
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678825
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