A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5866289



Internal ID9669844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68059584..68060486hg38UCSC Ensembl
chr15:68351922..68352824hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665979
Supporting Variants
SamplesNA19399
Known GenesPIAS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5866289
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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