A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv637e214



Internal ID22756531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72323900..72385275hg38UCSC Ensembl
chr18:69991135..70052510hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3861376
hg1961376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3643054, esv3643056
SamplesNA06984, HG03061, HG01498, HG01551, HG01137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv637e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer