A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13431834



Internal ID4809314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23908224..23916291hg38UCSC Ensembl
Innerchr9:23908224..23916291hg38UCSC Ensembl
Outerchr9:23908169..23916335hg38UCSC Ensembl
chr9:23908222..23916289hg19UCSC Ensembl
Innerchr9:23908222..23916289hg19UCSC Ensembl
Outerchr9:23908167..23916333hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg388068
hg198068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620022
Supporting Variants
SamplesNA11995
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13431834
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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