A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660384



Internal ID9579803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111970516..111970759hg38UCSC Ensembl
chr9:114732796..114733039hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6370382, essv5506930, essv6310556
SamplesHG01390, HG01101, NA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660384
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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