A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595944



Internal ID6983262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39961119..39978098hg38UCSC Ensembl
chr3:40002610..40019589hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3816980
hg1916980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv886e214
Supporting Variantsessv10987982
SamplesHG02406
Known GenesMYRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595944
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