A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1166e214



Internal ID22757060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15086335..15090692hg38UCSC Ensembl
chr6:15086566..15090923hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384358
hg194358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608161, esv3608162
SamplesNA06994
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1166e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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