A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664738



Internal ID9930843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24339432..24342165hg38UCSC Ensembl
Outerchr4:24339398..24342200hg38UCSC Ensembl
Innerchr4:24341055..24343788hg19UCSC Ensembl
Outerchr4:24341021..24343823hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382803
hg192803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv927e199
Supporting Variantsessv6269506
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664738
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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