A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624248



Internal ID7011104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94179058..94184515hg38UCSC Ensembl
Innerchr10:94179558..94184015hg38UCSC Ensembl
Outerchr10:94178058..94185515hg38UCSC Ensembl
chr10:95938815..95944272hg19UCSC Ensembl
Innerchr10:95939315..95943772hg19UCSC Ensembl
Outerchr10:95937815..95945272hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385458
hg195458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13902015, essv13902016
SamplesNA21125, HG00593
Known GenesPLCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624248
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