A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659283



Internal ID9925388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33848061..33851020hg38UCSC Ensembl
Innerchr4:33849683..33852642hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5654756, essv6556832
SamplesNA19239, NA19240
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659283
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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