A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624030



Internal ID6664197
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13881985
SamplesHG02589
Known GenesRGR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624030
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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