A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624535



Internal ID6664699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110249484..110250736hg38UCSC Ensembl
Innerchr10:110249514..110250706hg38UCSC Ensembl
Outerchr10:110249454..110250766hg38UCSC Ensembl
chr10:112009242..112010494hg19UCSC Ensembl
Innerchr10:112009272..112010464hg19UCSC Ensembl
Outerchr10:112009212..112010524hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933428
SamplesHG01807
Known GenesMXI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624535
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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