A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673999



Internal ID2907086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90792374..90793403hg38UCSC Ensembl
chr15:91335604..91336633hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5425377, essv5836360
SamplesNA19834, NA20289
Known GenesBLM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673999
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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