A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670542



Internal ID9936647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102106239..102115049hg38UCSC Ensembl
Outerchr3:102106082..102115202hg38UCSC Ensembl
Innerchr3:101825083..101833893hg19UCSC Ensembl
Outerchr3:101824926..101834046hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg389121
hg199121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5740236
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670542
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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