A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676494



Internal ID9942599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21761905..21770545hg38UCSC Ensembl
Outerchr3:21761868..21770595hg38UCSC Ensembl
Innerchr3:21803397..21812037hg19UCSC Ensembl
Outerchr3:21803360..21812087hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388728
hg198728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5436770, essv5817069
SamplesNA18538, HG00611
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676494
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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