A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13848746



Internal ID5594781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68085667..68094552hg38UCSC Ensembl
Innerchr10:68085676..68094544hg38UCSC Ensembl
Outerchr10:68085659..68094561hg38UCSC Ensembl
chr10:69845424..69854309hg19UCSC Ensembl
Innerchr10:69845433..69854301hg19UCSC Ensembl
Outerchr10:69845416..69854318hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg388886
hg198886
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623704
Supporting Variants
SamplesNA19030
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13848746
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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