A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623266



Internal ID7010123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52840276..52870553hg38UCSC Ensembl
Innerchr10:52840278..52870551hg38UCSC Ensembl
Outerchr10:52840274..52870555hg38UCSC Ensembl
chr10:54600036..54630313hg19UCSC Ensembl
Innerchr10:54600038..54630311hg19UCSC Ensembl
Outerchr10:54600034..54630315hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3830278
hg1930278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13810973
SamplesHG02102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623266
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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