A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5579873



Internal ID9212689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31110430..31111212hg38UCSC Ensembl
Outerchr19:31110393..31111262hg38UCSC Ensembl
Innerchr19:31601336..31602118hg19UCSC Ensembl
Outerchr19:31601299..31602168hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671042
Supporting Variants
SamplesNA07051
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5579873
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