A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv601e214



Internal ID22756495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11177300..11191319hg38UCSC Ensembl
chr18:11177299..11191318hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3814020
hg1914020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3641790, esv3641791
SamplesHG03073, HG00123, HG02239
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv601e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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