A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv18e214



Internal ID20121441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41880319..41885091hg38UCSC Ensembl
chr1:42345990..42350762hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3585834, esv3585832
SamplesHG03049, HG01198
Known GenesHIVEP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv18e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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