A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662751



Internal ID9928856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184972605..184987010hg38UCSC Ensembl
Outerchr4:184972555..184987068hg38UCSC Ensembl
Innerchr4:185893759..185908164hg19UCSC Ensembl
Outerchr4:185893709..185908222hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814514
hg1914514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6115981
SamplesNA19648
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662751
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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