A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv609e214



Internal ID22756503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27786844..27801779hg38UCSC Ensembl
chr18:25366808..25381743hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3814936
hg1914936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642048, esv3642049
SamplesHG01795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv609e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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