A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609909



Internal ID6996828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89820161..89824544hg38UCSC Ensembl
Innerchr6:89820211..89824494hg38UCSC Ensembl
Outerchr6:89819992..89824713hg38UCSC Ensembl
chr6:90529880..90534263hg19UCSC Ensembl
Innerchr6:90529930..90534213hg19UCSC Ensembl
Outerchr6:90529711..90534432hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384384
hg194384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12459744
SamplesNA20355
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609909
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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