A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669238



Internal ID9935343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24339612..24341965hg38UCSC Ensembl
Outerchr4:24339429..24342162hg38UCSC Ensembl
Innerchr4:24341235..24343588hg19UCSC Ensembl
Outerchr4:24341052..24343785hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv927e199
Supporting Variantsessv6251944
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669238
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