A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6269506



Internal ID8792867
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 Flag1
Merged StatusS
Merged Variantsesv2664738
Supporting Variants
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6269506
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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