A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624636



Internal ID7011487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115496407..115499422hg38UCSC Ensembl
Innerchr10:115496432..115499397hg38UCSC Ensembl
Outerchr10:115496382..115499447hg38UCSC Ensembl
chr10:117255917..117258932hg19UCSC Ensembl
Innerchr10:117255942..117258907hg19UCSC Ensembl
Outerchr10:117255892..117258957hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13943534, essv13943533
SamplesHG02356, HG02379
Known GenesATRNL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624636
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