A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659872



Internal ID9925977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25615721..25620035hg38UCSC Ensembl
Outerchr4:25615564..25620188hg38UCSC Ensembl
Innerchr4:25617343..25621657hg19UCSC Ensembl
Outerchr4:25617186..25621810hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384625
hg194625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6583842
SamplesHG01197
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659872
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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