A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623886



Internal ID7010742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78089919..78098100hg38UCSC Ensembl
Innerchr10:78089919..78098100hg38UCSC Ensembl
Outerchr10:78089753..78098269hg38UCSC Ensembl
chr10:79849676..79857857hg19UCSC Ensembl
Innerchr10:79849676..79857857hg19UCSC Ensembl
Outerchr10:79849510..79858026hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg388182
hg198182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866617, essv13866615, essv13866611, essv13866619, essv13866614, essv13866622, essv13866612, essv13866625, essv13866621, essv13866616, essv13866620, essv13866623, essv13866610, essv13866618, essv13866624, essv13866613
SamplesHG02375, HG00457, HG01809, HG02151, NA18645, HG02136, HG01857, HG00598, NA18572, HG01852, HG00684, NA18536, HG00623, HG01798, HG02371, NA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623886
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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