A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663193



Internal ID9929298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56225576..56239994hg38UCSC Ensembl
chr15:56517774..56532192hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814419
hg1914419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5716010
SamplesNA19428
Known GenesRFX7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663193
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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