A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv600e214



Internal ID22756494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10325236..10347699hg38UCSC Ensembl
chr18:10325233..10347696hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3822464
hg1922464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3641773, esv3641774
SamplesNA21097, HG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv600e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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