A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5568707



Internal ID8916770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35469000..35470130hg38UCSC Ensembl
chr15:35761201..35762331hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665398
Supporting Variants
SamplesHG00418
Known GenesDPH6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5568707
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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