A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671479



Internal ID9937584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73687239..73687949hg38UCSC Ensembl
Outerchr3:73687202..73687999hg38UCSC Ensembl
Innerchr3:73736390..73737100hg19UCSC Ensembl
Outerchr3:73736353..73737150hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6335908
SamplesHG00309
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671479
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