A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656880



Internal ID9922985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46613208..46614768hg38UCSC Ensembl
chr3:46654698..46656258hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5938922
SamplesNA19054
Known GenesLOC100132146
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656880
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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