A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663720



Internal ID9929825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12288536..12588772hg38UCSC Ensembl
Outerchr9:12288502..12588807hg38UCSC Ensembl
Innerchr9:12288536..12588772hg19UCSC Ensembl
Outerchr9:12288502..12588807hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38300306
hg19300306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5517472
SamplesNA19130
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663720
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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