A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666605



Internal ID9932710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67287523..67290748hg38UCSC Ensembl
chr15:67579861..67583086hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383226
hg193226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5483468, essv5571143
SamplesHG01351, NA19661
Known GenesIQCH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666605
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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