A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671324



Internal ID9937429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93354678..93362723hg38UCSC Ensembl
chr9:96116960..96125005hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg388046
hg198046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5533695, essv5399031, essv5539870, essv5660430, essv6038776
SamplesNA20340, NA19901, NA19449, NA19440, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671324
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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