A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669350



Internal ID9935455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:101777347..101784979hg38UCSC Ensembl
Innerchr2:102393809..102401441hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg387633
hg197633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5655914
SamplesNA19238
Known GenesMAP4K4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669350
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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