A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622499



Internal ID7009358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18071053..18072880hg38UCSC Ensembl
Innerchr10:18071096..18072838hg38UCSC Ensembl
Outerchr10:18071011..18072923hg38UCSC Ensembl
chr10:18359982..18361809hg19UCSC Ensembl
Innerchr10:18360025..18361767hg19UCSC Ensembl
Outerchr10:18359940..18361852hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13708100
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622499
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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