A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5902033



Internal ID8731985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882868..82888918hg38UCSC Ensembl
chr15:83551620..83557670hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661148
Supporting Variants
SamplesHG00118
Known GenesHOMER2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5902033
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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