A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671876



Internal ID9937981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1192001..1571212hg38UCSC Ensembl
chr9:1192001..1571212hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38379212
hg19379212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5713605
SamplesNA18873
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671876
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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