A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599094



Internal ID6639360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191225726..191310300hg38UCSC Ensembl
Innerchr3:191225761..191310266hg38UCSC Ensembl
Outerchr3:191225692..191310335hg38UCSC Ensembl
chr3:190943515..191028089hg19UCSC Ensembl
Innerchr3:190943550..191028055hg19UCSC Ensembl
Outerchr3:190943481..191028124hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3884575
hg1984575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11269509, essv11269510
SamplesHG01791, HG01920
Known GenesOSTN, UTS2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599094
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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