A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609808



Internal ID6996727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84981032..84994986hg38UCSC Ensembl
chr6:85690750..85704704hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3813955
hg1913955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454381, essv12454382
SamplesHG01918, HG01977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609808
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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