A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764238



Internal ID4700584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43341317..43349518hg38UCSC Ensembl
Innerchr10:43341367..43349468hg38UCSC Ensembl
Outerchr10:43341263..43349572hg38UCSC Ensembl
chr10:43836765..43844966hg19UCSC Ensembl
Innerchr10:43836815..43844916hg19UCSC Ensembl
Outerchr10:43836711..43845020hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623040
Supporting Variants
SamplesHG04219
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764238
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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