A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622681



Internal ID7009539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898912..25903165hg38UCSC Ensembl
Innerchr10:25898912..25903165hg38UCSC Ensembl
Outerchr10:25898668..25903424hg38UCSC Ensembl
chr10:26187841..26192094hg19UCSC Ensembl
Innerchr10:26187841..26192094hg19UCSC Ensembl
Outerchr10:26187597..26192353hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv103e214
Supporting Variantsessv13728168, essv13728169
SamplesNA20586, NA18950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622681
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