A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1162e214



Internal ID22757056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3159187..3179207hg38UCSC Ensembl
chr6:3159421..3179441hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3820021
hg1920021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3607922, esv3607923
SamplesNA19917, NA19143, NA19248
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1162e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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