A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13594376



Internal ID6319100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107473221..107476141hg38UCSC Ensembl
Innerchr9:107473221..107476141hg38UCSC Ensembl
Outerchr9:107473076..107476253hg38UCSC Ensembl
chr9:110235502..110238422hg19UCSC Ensembl
Innerchr9:110235502..110238422hg19UCSC Ensembl
Outerchr9:110235357..110238534hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382921
hg192921
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621399
Supporting Variants
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13594376
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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