A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666768



Internal ID9932873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40823402..40900119hg38UCSC Ensembl
Outerchr9:40823368..40900154hg38UCSC Ensembl
Innerchr9:66776430..66853147hg19UCSC Ensembl
Outerchr9:66776396..66853182hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3876787
hg1976787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5783980
SamplesNA19058
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666768
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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