A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660617



Internal ID9926722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159389915..159391562hg38UCSC Ensembl
Outerchr4:159389758..159391715hg38UCSC Ensembl
Innerchr4:160311067..160312714hg19UCSC Ensembl
Outerchr4:160310910..160312867hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381958
hg191958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5657569, essv5407651
SamplesNA19058, NA19063
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660617
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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