A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678006



Internal ID9944111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15129932..15130238hg38UCSC Ensembl
chr4:15131556..15131862hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6255791, essv5461387, essv6376511, essv6449184, essv6585447
SamplesNA12275, NA18990, NA20755, NA20765, NA20528
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678006
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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