A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610287



Internal ID6997204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106841611..106852459hg38UCSC Ensembl
chr6:107289486..107300334hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3810849
hg1910849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499080
SamplesHG03445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610287
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