A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1168e214



Internal ID22757062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18753803..18759861hg38UCSC Ensembl
chr6:18754034..18760092hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386059
hg196059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608249, esv3608251
SamplesHG03074, NA20905, NA19235, NA19317, NA19725, NA19788, HG02497, NA18853, NA20801, NA19331
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1168e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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