A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13870363



Internal ID5889427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80228093..80234185hg38UCSC Ensembl
Innerchr10:80228093..80234185hg38UCSC Ensembl
Outerchr10:80227593..80234685hg38UCSC Ensembl
chr10:81987849..81993941hg19UCSC Ensembl
Innerchr10:81987849..81993941hg19UCSC Ensembl
Outerchr10:81987349..81994441hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386093
hg196093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623950
Supporting Variants
SamplesNA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13870363
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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