A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662859



Internal ID9928964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27672066..27676779hg38UCSC Ensembl
Outerchr3:27671909..27676932hg38UCSC Ensembl
Innerchr3:27713557..27718270hg19UCSC Ensembl
Outerchr3:27713400..27718423hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385024
hg195024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5958820
SamplesHG00476
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662859
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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