A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1199e214



Internal ID22757093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85667280..85673116hg38UCSC Ensembl
chr6:86376998..86382834hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg385837
hg195837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3609821, esv3609820
SamplesHG02134
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1199e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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