A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv886e214



Internal ID22756780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39956794..39978098hg38UCSC Ensembl
chr3:39998285..40019589hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3821305
hg1921305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595944, esv3595942
SamplesHG00699, HG02406
Known GenesMYRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv886e214
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