A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668014



Internal ID2901101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:213062..213392hg38UCSC Ensembl
chr7:213062..213392hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5451278, essv5954580
SamplesNA19707, HG00278
Known GenesFAM20C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
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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