A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6449184



Internal ID9858902
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 StatusS
Merged Variantsesv2678006
Supporting Variants
SamplesNA20528
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6449184
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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