A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673999



Internal ID4718333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91335604..91336633hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv5425377, essv5836360
SamplesNA19834, NA20289
Known GenesBLM
Method
Analysis
Platform
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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