A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609793



Internal ID6996713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84323942..84512334hg38UCSC Ensembl
chr6:85033660..85222052hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38188393
hg19188393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454102
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609793
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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