A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661430



Internal ID9927535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88405252..88414545hg38UCSC Ensembl
chr9:91020167..91029460hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389294
hg199294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5431124, essv5883704
SamplesNA19311, NA19360
Known GenesSPIN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661430
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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