A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662096



Internal ID9928201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132040001..132045704hg38UCSC Ensembl
chr9:134915388..134921091hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385704
hg195704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5749798
SamplesNA19007
Known GenesMED27
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662096
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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