A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660468



Internal ID9579887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104833898..104835056hg38UCSC Ensembl
Outerchr9:104833861..104835106hg38UCSC Ensembl
Innerchr9:107596179..107597337hg19UCSC Ensembl
Outerchr9:107596142..107597387hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1366e199
Supporting Variantsessv5856567
SamplesNA19717
Known GenesABCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660468
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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