A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610411



Internal ID6997328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113323981..113328966hg38UCSC Ensembl
chr6:113645183..113650168hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384986
hg194986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1211e214
Supporting Variantsessv12505919, essv12505918
SamplesHG01443, HG01550
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610411
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