A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1171e214



Internal ID22757065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27846413..27862239hg38UCSC Ensembl
chr6:27814191..27830017hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3815827
hg1915827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608443, esv3608442
SamplesHG02040
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1171e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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