A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668318



Internal ID9934423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34904642..34905658hg38UCSC Ensembl
chr15:35196843..35197859hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6151198, essv6304185, essv5440838, essv6407789, essv5950808, essv6003925, essv6490324, essv5588281
SamplesNA19393, NA19404, NA19908, NA19247, NA19391, NA19428, NA19311, NA19467
Known GenesAQR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668318
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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