A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659171



Internal ID9925276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42286137..42303428hg38UCSC Ensembl
Outerchr3:42286100..42303478hg38UCSC Ensembl
Innerchr3:42327629..42344920hg19UCSC Ensembl
Outerchr3:42327592..42344970hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3817379
hg1917379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5767670
SamplesNA19726
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659171
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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