A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13881985



Internal ID3883801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84248220..84249061hg38UCSC Ensembl
Innerchr10:84248226..84249056hg38UCSC Ensembl
Outerchr10:84248215..84249067hg38UCSC Ensembl
chr10:86007976..86008817hg19UCSC Ensembl
Innerchr10:86007982..86008812hg19UCSC Ensembl
Outerchr10:86007971..86008823hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624030
Supporting Variants
SamplesHG02589
Known GenesRGR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13881985
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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