A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1266e214



Internal ID22757160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12889606..12952303hg38UCSC Ensembl
chr7:12929231..12991928hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3862698
hg1962698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612269, esv3612271
SamplesNA20911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1266e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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