A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3335904



Internal ID15182893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106010584..106012682hg38UCSC Ensembl
Innerchr6:106011584..106011682hg38UCSC Ensembl
Outerchr6:106009584..106013682hg38UCSC Ensembl
chr6:106458459..106460557hg19UCSC Ensembl
Innerchr6:106459459..106459557hg19UCSC Ensembl
Outerchr6:106457459..106461557hg19UCSC Ensembl
chr6:106565152..106567250hg18UCSC Ensembl
Innerchr6:106566152..106566250hg18UCSC Ensembl
Outerchr6:106564152..106568250hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3610e59
Supporting Variantsessv8695010
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3335904
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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