A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622485



Internal ID6662655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17365070..17369491hg38UCSC Ensembl
Innerchr10:17365094..17369467hg38UCSC Ensembl
Outerchr10:17365046..17369515hg38UCSC Ensembl
chr10:17407069..17411490hg19UCSC Ensembl
Innerchr10:17407093..17411466hg19UCSC Ensembl
Outerchr10:17407045..17411514hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13707014, essv13707015
SamplesHG01705, HG03397
Known GenesST8SIA6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622485
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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