A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623891



Internal ID7010747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78383546..78384646hg38UCSC Ensembl
Innerchr10:78383547..78384645hg38UCSC Ensembl
Outerchr10:78383545..78384647hg38UCSC Ensembl
chr10:80143303..80144403hg19UCSC Ensembl
Innerchr10:80143304..80144402hg19UCSC Ensembl
Outerchr10:80143302..80144404hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866649, essv13866660, essv13866659, essv13866652, essv13866648, essv13866655, essv13866643, essv13866664, essv13866653, essv13866656, essv13866661, essv13866662, essv13866658, essv13866644, essv13866650, essv13866651, essv13866645, essv13866646, essv13866642, essv13866663, essv13866654, essv13866647, essv13866657
SamplesHG03559, HG03052, NA19204, NA18861, HG02852, HG03115, HG03126, HG03436, HG02981, HG02819, HG02479, HG03363, HG02449, HG02968, HG02429, NA18879, NA18865, HG03473, HG02095, HG03445, HG02861, HG02465, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623891
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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