A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623020



Internal ID7009877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42641343..42709650hg38UCSC Ensembl
Innerchr10:42641343..42709650hg38UCSC Ensembl
Outerchr10:42640843..42710150hg38UCSC Ensembl
chr10:43136791..43205098hg19UCSC Ensembl
Innerchr10:43136791..43205098hg19UCSC Ensembl
Outerchr10:43136291..43205598hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3868308
hg1968308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764065
SamplesNA18620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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