A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676450



Internal ID9942555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87899433..87956945hg38UCSC Ensembl
chr3:87948583..88006095hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3857513
hg1957513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5941436
SamplesHG01389
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676450
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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