A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678855



Internal ID9598274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77400770..77401651hg38UCSC Ensembl
Outerchr3:77400736..77401686hg38UCSC Ensembl
Innerchr3:77449921..77450802hg19UCSC Ensembl
Outerchr3:77449887..77450837hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5454747
SamplesHG00152
Known GenesROBO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678855
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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