A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621422



Internal ID7008291
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594860
SamplesHG03960
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621422
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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