A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv366e214



Internal ID22756260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105573410..105657283hg38UCSC Ensembl
chr13:106225759..106309632hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3883874
hg1983874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633448, esv3633447
SamplesNA19789, HG01149, NA19783
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv366e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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