A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657029



Internal ID4701363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191960764..192028714hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv5854759
SamplesNA19346
Known GenesSTAT4
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657029
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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