A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660163



Internal ID9579582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:67587857..67588507hg38UCSC Ensembl
Outerchr4:67587820..67588557hg38UCSC Ensembl
Innerchr4:68453575..68454225hg19UCSC Ensembl
Outerchr4:68453538..68454275hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817762
SamplesNA18597
Known GenesSTAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660163
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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