A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1378e214



Internal ID22757272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13312741..13394970hg38UCSC Ensembl
chr8:13170250..13252479hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3882230
hg1982230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3616306, esv3616304
SamplesHG02819
Known GenesDLC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1378e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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