A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663504



Internal ID9929609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3032759..3084599hg38UCSC Ensembl
chr2:3036531..3088371hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3851841
hg1951841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5796442
SamplesNA19469
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663504
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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