A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13594860



Internal ID4453885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108652161..108666032hg38UCSC Ensembl
Innerchr9:108652177..108666016hg38UCSC Ensembl
Outerchr9:108652145..108666048hg38UCSC Ensembl
chr9:111414441..111428312hg19UCSC Ensembl
Innerchr9:111414457..111428296hg19UCSC Ensembl
Outerchr9:111414425..111428328hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3813872
hg1913872
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621422
Supporting Variants
SamplesHG03960
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13594860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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