A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668014



Internal ID4712348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:213062..213392hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv5451278, essv5954580
SamplesNA19707, HG00278
Known GenesFAM20C
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668014
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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