A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608285



Internal ID6995215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20073757..20088831hg38UCSC Ensembl
Innerchr6:20073780..20088808hg38UCSC Ensembl
Outerchr6:20073734..20088854hg38UCSC Ensembl
chr6:20073988..20089062hg19UCSC Ensembl
Innerchr6:20074011..20089039hg19UCSC Ensembl
Outerchr6:20073965..20089085hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3815075
hg1915075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12215649, essv12215650
SamplesHG04018, HG04047
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608285
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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