A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624628



Internal ID7011479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114959761..114970998hg38UCSC Ensembl
Innerchr10:114959811..114970948hg38UCSC Ensembl
Outerchr10:114959691..114971068hg38UCSC Ensembl
chr10:116719520..116730757hg19UCSC Ensembl
Innerchr10:116719570..116730707hg19UCSC Ensembl
Outerchr10:116719450..116730827hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811238
hg1911238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13941473
SamplesHG00524
Known GenesTRUB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624628
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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