A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665398



Internal ID9931503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35469000..35470130hg38UCSC Ensembl
chr15:35761201..35762331hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5568707
SamplesHG00418
Known GenesDPH6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665398
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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