A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660399



Internal ID9926504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36670300..36677851hg38UCSC Ensembl
Outerchr3:36670143..36678004hg38UCSC Ensembl
Innerchr3:36711791..36719342hg19UCSC Ensembl
Outerchr3:36711634..36719495hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387862
hg197862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6036936
SamplesNA18909
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660399
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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