A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1161e214



Internal ID22757055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1135847..1213954hg38UCSC Ensembl
chr6:1136082..1214189hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3878108
hg1978108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3607882, esv3607884
SamplesHG03917, HG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1161e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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